Nonregistration, discontinuation, and nonpublication of randomized trials: A repeated metaresearch analysis

We previously found that 25% of 1,017 randomized clinical trials (RCTs) approved between 2000 and 2003 were discontinued prematurely, and 44% remained unpublished at a median of 12 years follow-up. We aimed to assess a decade later (1) whether rates of completion and publication have increased; (2)...

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Veröffentlicht in:PLoS medicine 2022-04, Vol.19 (4), p.e1003980-e1003980
Hauptverfasser: Speich, Benjamin, Gryaznov, Dmitry, Busse, Jason W, Gloy, Viktoria L, Lohner, Szimonetta, Klatte, Katharina, Taji Heravi, Ala, Ghosh, Nilabh, Lee, Hopin, Mansouri, Anita, Marian, Ioana R, Saccilotto, Ramon, Nury, Edris, Kasenda, Benjamin, Ojeda-Ruiz, Elena, Schandelmaier, Stefan, Tomonaga, Yuki, Amstutz, Alain, Pauli-Magnus, Christiane, Bischoff, Karin, Wollmann, Katharina, Rehner, Laura, Meerpohl, Joerg J, Nordmann, Alain, Wong, Jacqueline, Chow, Ngai, Hong, Patrick Jiho, Mc Cord-De Iaco, Kimberly, Sricharoenchai, Sirintip, Agarwal, Arnav, Schwenkglenks, Matthias, Hemkens, Lars G, von Elm, Erik, Copsey, Bethan, Griessbach, Alexandra N, Schönenberger, Christof, Mertz, Dominik, Blümle, Anette, von Niederhäusern, Belinda, Hopewell, Sally, Odutayo, Ayodele, Briel, Matthias
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container_issue 4
container_start_page e1003980
container_title PLoS medicine
container_volume 19
creator Speich, Benjamin
Gryaznov, Dmitry
Busse, Jason W
Gloy, Viktoria L
Lohner, Szimonetta
Klatte, Katharina
Taji Heravi, Ala
Ghosh, Nilabh
Lee, Hopin
Mansouri, Anita
Marian, Ioana R
Saccilotto, Ramon
Nury, Edris
Kasenda, Benjamin
Ojeda-Ruiz, Elena
Schandelmaier, Stefan
Tomonaga, Yuki
Amstutz, Alain
Pauli-Magnus, Christiane
Bischoff, Karin
Wollmann, Katharina
Rehner, Laura
Meerpohl, Joerg J
Nordmann, Alain
Wong, Jacqueline
Chow, Ngai
Hong, Patrick Jiho
Mc Cord-De Iaco, Kimberly
Sricharoenchai, Sirintip
Agarwal, Arnav
Schwenkglenks, Matthias
Hemkens, Lars G
von Elm, Erik
Copsey, Bethan
Griessbach, Alexandra N
Schönenberger, Christof
Mertz, Dominik
Blümle, Anette
von Niederhäusern, Belinda
Hopewell, Sally
Odutayo, Ayodele
Briel, Matthias
description We previously found that 25% of 1,017 randomized clinical trials (RCTs) approved between 2000 and 2003 were discontinued prematurely, and 44% remained unpublished at a median of 12 years follow-up. We aimed to assess a decade later (1) whether rates of completion and publication have increased; (2) the extent to which nonpublished RCTs can be identified in trial registries; and (3) the association between reporting quality of protocols and premature discontinuation or nonpublication of RCTs. We included 326 RCT protocols approved in 2012 by research ethics committees in Switzerland, the United Kingdom, Germany, and Canada in this metaresearch study. Pilot, feasibility, and phase 1 studies were excluded. We extracted trial characteristics from each study protocol and systematically searched for corresponding trial registration (if not reported in the protocol) and full text publications until February 2022. For trial registrations, we searched the (i) World Health Organization: International Clinical Trial Registry Platform (ICTRP); (ii) US National Library of Medicine (ClinicalTrials.gov); (iii) European Union Drug Regulating Authorities Clinical Trials Database (EUCTR); (iv) ISRCTN registry; and (v) Google. For full text publications, we searched PubMed, Google Scholar, and Scopus. We recorded whether RCTs were registered, discontinued (including reason for discontinuation), and published. The reporting quality of RCT protocols was assessed with the 33-item SPIRIT checklist. We used multivariable logistic regression to examine the association between the independent variables protocol reporting quality, planned sample size, type of control (placebo versus other), reporting of any recruitment projection, single-center versus multicenter trials, and industry versus investigator sponsoring, with the 2 dependent variables: (1) publication of RCT results; and (2) trial discontinuation due to poor recruitment. Of the 326 included trials, 19 (6%) were unregistered. Ninety-eight trials (30%) were discontinued prematurely, most often due to poor recruitment (37%; 36/98). One in 5 trials (21%; 70/326) remained unpublished at 10 years follow-up, and 21% of unpublished trials (15/70) were unregistered. Twenty-three of 147 investigator-sponsored trials (16%) reported their results in a trial registry in contrast to 150 of 179 industry-sponsored trials (84%). The median proportion of reported SPIRIT items in included RCT protocols was 69% (interquartile range 61% to 77
doi_str_mv 10.1371/journal.pmed.1003980
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We aimed to assess a decade later (1) whether rates of completion and publication have increased; (2) the extent to which nonpublished RCTs can be identified in trial registries; and (3) the association between reporting quality of protocols and premature discontinuation or nonpublication of RCTs. We included 326 RCT protocols approved in 2012 by research ethics committees in Switzerland, the United Kingdom, Germany, and Canada in this metaresearch study. Pilot, feasibility, and phase 1 studies were excluded. We extracted trial characteristics from each study protocol and systematically searched for corresponding trial registration (if not reported in the protocol) and full text publications until February 2022. For trial registrations, we searched the (i) World Health Organization: International Clinical Trial Registry Platform (ICTRP); (ii) US National Library of Medicine (ClinicalTrials.gov); (iii) European Union Drug Regulating Authorities Clinical Trials Database (EUCTR); (iv) ISRCTN registry; and (v) Google. For full text publications, we searched PubMed, Google Scholar, and Scopus. We recorded whether RCTs were registered, discontinued (including reason for discontinuation), and published. The reporting quality of RCT protocols was assessed with the 33-item SPIRIT checklist. We used multivariable logistic regression to examine the association between the independent variables protocol reporting quality, planned sample size, type of control (placebo versus other), reporting of any recruitment projection, single-center versus multicenter trials, and industry versus investigator sponsoring, with the 2 dependent variables: (1) publication of RCT results; and (2) trial discontinuation due to poor recruitment. Of the 326 included trials, 19 (6%) were unregistered. Ninety-eight trials (30%) were discontinued prematurely, most often due to poor recruitment (37%; 36/98). One in 5 trials (21%; 70/326) remained unpublished at 10 years follow-up, and 21% of unpublished trials (15/70) were unregistered. Twenty-three of 147 investigator-sponsored trials (16%) reported their results in a trial registry in contrast to 150 of 179 industry-sponsored trials (84%). The median proportion of reported SPIRIT items in included RCT protocols was 69% (interquartile range 61% to 77%). We found no variables associated with trial discontinuation; however, lower reporting quality of trial protocols was associated with nonpublication (odds ratio, 0.71 for each 10% increment in the proportion of SPIRIT items met; 95% confidence interval, 0.55 to 0.92; p = 0.009). Study limitations include that the moderate sample size may have limited the ability of our regression models to identify significant associations. We have observed that rates of premature trial discontinuation have not changed in the past decade. Nonpublication of RCTs has declined but remains common; 21% of unpublished trials could not be identified in registries. Only 16% of investigator-sponsored trials reported results in a trial registry. Higher reporting quality of RCT protocols was associated with publication of results. Further efforts from all stakeholders are needed to improve efficiency and transparency of clinical research.</description><identifier>ISSN: 1549-1676</identifier><identifier>ISSN: 1549-1277</identifier><identifier>EISSN: 1549-1676</identifier><identifier>DOI: 10.1371/journal.pmed.1003980</identifier><identifier>PMID: 35476675</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Clinical trials ; Data collection ; Feasibility studies ; Germany ; Humans ; Intervention ; Management ; Medical research ; Medicine and Health Sciences ; Medicine, Experimental ; Methods ; Odds Ratio ; Patients ; Randomized Controlled Trials as Topic ; Registration ; Registries ; Regression analysis ; Research and Analysis Methods ; Research ethics ; Research Personnel ; Science Policy ; Statistics ; Variables</subject><ispartof>PLoS medicine, 2022-04, Vol.19 (4), p.e1003980-e1003980</ispartof><rights>COPYRIGHT 2022 Public Library of Science</rights><rights>2022 Speich et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 Speich et al 2022 Speich et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c764t-438c8575a3ada0b03728d6a27dbc81eff8f75668b738549f2b519fa4454df5ec3</citedby><cites>FETCH-LOGICAL-c764t-438c8575a3ada0b03728d6a27dbc81eff8f75668b738549f2b519fa4454df5ec3</cites><orcidid>0000-0002-4438-4961 ; 0000-0003-3726-1856 ; 0000-0002-6292-4802 ; 0000-0001-7853-4967 ; 0000-0002-7583-8137 ; 0000-0002-8429-0337 ; 0000-0002-0692-8112 ; 0000-0003-1716-993X ; 0000-0003-4337-1613 ; 0000-0003-2877-1029 ; 0000-0001-7217-1173 ; 0000-0002-2361-6794 ; 0000-0003-3752-1611 ; 0000-0002-4620-7010 ; 0000-0002-1333-5403 ; 0000-0002-0931-7851 ; 0000-0003-0110-8585 ; 0000-0002-7500-1636 ; 0000-0002-2070-5230 ; 0000-0003-1710-5450 ; 0000-0002-9856-3500 ; 0000-0002-0178-8712 ; 0000-0002-7412-0406 ; 0000-0001-5098-0375 ; 0000-0002-3444-1432 ; 0000-0001-5692-0314 ; 0000-0002-2147-3160 ; 0000-0002-3301-8085 ; 0000-0001-9783-6549</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9094518/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9094518/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79342,79343</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35476675$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Speich, Benjamin</creatorcontrib><creatorcontrib>Gryaznov, Dmitry</creatorcontrib><creatorcontrib>Busse, Jason W</creatorcontrib><creatorcontrib>Gloy, Viktoria L</creatorcontrib><creatorcontrib>Lohner, Szimonetta</creatorcontrib><creatorcontrib>Klatte, Katharina</creatorcontrib><creatorcontrib>Taji Heravi, Ala</creatorcontrib><creatorcontrib>Ghosh, Nilabh</creatorcontrib><creatorcontrib>Lee, Hopin</creatorcontrib><creatorcontrib>Mansouri, Anita</creatorcontrib><creatorcontrib>Marian, Ioana R</creatorcontrib><creatorcontrib>Saccilotto, Ramon</creatorcontrib><creatorcontrib>Nury, Edris</creatorcontrib><creatorcontrib>Kasenda, Benjamin</creatorcontrib><creatorcontrib>Ojeda-Ruiz, Elena</creatorcontrib><creatorcontrib>Schandelmaier, Stefan</creatorcontrib><creatorcontrib>Tomonaga, Yuki</creatorcontrib><creatorcontrib>Amstutz, Alain</creatorcontrib><creatorcontrib>Pauli-Magnus, Christiane</creatorcontrib><creatorcontrib>Bischoff, Karin</creatorcontrib><creatorcontrib>Wollmann, Katharina</creatorcontrib><creatorcontrib>Rehner, Laura</creatorcontrib><creatorcontrib>Meerpohl, Joerg J</creatorcontrib><creatorcontrib>Nordmann, Alain</creatorcontrib><creatorcontrib>Wong, Jacqueline</creatorcontrib><creatorcontrib>Chow, Ngai</creatorcontrib><creatorcontrib>Hong, Patrick Jiho</creatorcontrib><creatorcontrib>Mc Cord-De Iaco, Kimberly</creatorcontrib><creatorcontrib>Sricharoenchai, Sirintip</creatorcontrib><creatorcontrib>Agarwal, Arnav</creatorcontrib><creatorcontrib>Schwenkglenks, Matthias</creatorcontrib><creatorcontrib>Hemkens, Lars G</creatorcontrib><creatorcontrib>von Elm, Erik</creatorcontrib><creatorcontrib>Copsey, Bethan</creatorcontrib><creatorcontrib>Griessbach, Alexandra N</creatorcontrib><creatorcontrib>Schönenberger, Christof</creatorcontrib><creatorcontrib>Mertz, Dominik</creatorcontrib><creatorcontrib>Blümle, Anette</creatorcontrib><creatorcontrib>von Niederhäusern, Belinda</creatorcontrib><creatorcontrib>Hopewell, Sally</creatorcontrib><creatorcontrib>Odutayo, Ayodele</creatorcontrib><creatorcontrib>Briel, Matthias</creatorcontrib><title>Nonregistration, discontinuation, and nonpublication of randomized trials: A repeated metaresearch analysis</title><title>PLoS medicine</title><addtitle>PLoS Med</addtitle><description>We previously found that 25% of 1,017 randomized clinical trials (RCTs) approved between 2000 and 2003 were discontinued prematurely, and 44% remained unpublished at a median of 12 years follow-up. We aimed to assess a decade later (1) whether rates of completion and publication have increased; (2) the extent to which nonpublished RCTs can be identified in trial registries; and (3) the association between reporting quality of protocols and premature discontinuation or nonpublication of RCTs. We included 326 RCT protocols approved in 2012 by research ethics committees in Switzerland, the United Kingdom, Germany, and Canada in this metaresearch study. Pilot, feasibility, and phase 1 studies were excluded. We extracted trial characteristics from each study protocol and systematically searched for corresponding trial registration (if not reported in the protocol) and full text publications until February 2022. For trial registrations, we searched the (i) World Health Organization: International Clinical Trial Registry Platform (ICTRP); (ii) US National Library of Medicine (ClinicalTrials.gov); (iii) European Union Drug Regulating Authorities Clinical Trials Database (EUCTR); (iv) ISRCTN registry; and (v) Google. For full text publications, we searched PubMed, Google Scholar, and Scopus. We recorded whether RCTs were registered, discontinued (including reason for discontinuation), and published. The reporting quality of RCT protocols was assessed with the 33-item SPIRIT checklist. We used multivariable logistic regression to examine the association between the independent variables protocol reporting quality, planned sample size, type of control (placebo versus other), reporting of any recruitment projection, single-center versus multicenter trials, and industry versus investigator sponsoring, with the 2 dependent variables: (1) publication of RCT results; and (2) trial discontinuation due to poor recruitment. Of the 326 included trials, 19 (6%) were unregistered. Ninety-eight trials (30%) were discontinued prematurely, most often due to poor recruitment (37%; 36/98). One in 5 trials (21%; 70/326) remained unpublished at 10 years follow-up, and 21% of unpublished trials (15/70) were unregistered. Twenty-three of 147 investigator-sponsored trials (16%) reported their results in a trial registry in contrast to 150 of 179 industry-sponsored trials (84%). The median proportion of reported SPIRIT items in included RCT protocols was 69% (interquartile range 61% to 77%). We found no variables associated with trial discontinuation; however, lower reporting quality of trial protocols was associated with nonpublication (odds ratio, 0.71 for each 10% increment in the proportion of SPIRIT items met; 95% confidence interval, 0.55 to 0.92; p = 0.009). Study limitations include that the moderate sample size may have limited the ability of our regression models to identify significant associations. We have observed that rates of premature trial discontinuation have not changed in the past decade. Nonpublication of RCTs has declined but remains common; 21% of unpublished trials could not be identified in registries. Only 16% of investigator-sponsored trials reported results in a trial registry. Higher reporting quality of RCT protocols was associated with publication of results. Further efforts from all stakeholders are needed to improve efficiency and transparency of clinical research.</description><subject>Clinical trials</subject><subject>Data collection</subject><subject>Feasibility studies</subject><subject>Germany</subject><subject>Humans</subject><subject>Intervention</subject><subject>Management</subject><subject>Medical research</subject><subject>Medicine and Health Sciences</subject><subject>Medicine, Experimental</subject><subject>Methods</subject><subject>Odds Ratio</subject><subject>Patients</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Registration</subject><subject>Registries</subject><subject>Regression analysis</subject><subject>Research and Analysis Methods</subject><subject>Research ethics</subject><subject>Research Personnel</subject><subject>Science 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discontinuation, and nonpublication of randomized trials: A repeated metaresearch analysis</title><author>Speich, Benjamin ; Gryaznov, Dmitry ; Busse, Jason W ; Gloy, Viktoria L ; Lohner, Szimonetta ; Klatte, Katharina ; Taji Heravi, Ala ; Ghosh, Nilabh ; Lee, Hopin ; Mansouri, Anita ; Marian, Ioana R ; Saccilotto, Ramon ; Nury, Edris ; Kasenda, Benjamin ; Ojeda-Ruiz, Elena ; Schandelmaier, Stefan ; Tomonaga, Yuki ; Amstutz, Alain ; Pauli-Magnus, Christiane ; Bischoff, Karin ; Wollmann, Katharina ; Rehner, Laura ; Meerpohl, Joerg J ; Nordmann, Alain ; Wong, Jacqueline ; Chow, Ngai ; Hong, Patrick Jiho ; Mc Cord-De Iaco, Kimberly ; Sricharoenchai, Sirintip ; Agarwal, Arnav ; Schwenkglenks, Matthias ; Hemkens, Lars G ; von Elm, Erik ; Copsey, Bethan ; Griessbach, Alexandra N ; Schönenberger, Christof ; Mertz, Dominik ; Blümle, Anette ; von Niederhäusern, Belinda ; Hopewell, Sally ; Odutayo, Ayodele ; Briel, 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Policy</topic><topic>Statistics</topic><topic>Variables</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Speich, Benjamin</creatorcontrib><creatorcontrib>Gryaznov, Dmitry</creatorcontrib><creatorcontrib>Busse, Jason W</creatorcontrib><creatorcontrib>Gloy, Viktoria L</creatorcontrib><creatorcontrib>Lohner, Szimonetta</creatorcontrib><creatorcontrib>Klatte, Katharina</creatorcontrib><creatorcontrib>Taji Heravi, Ala</creatorcontrib><creatorcontrib>Ghosh, Nilabh</creatorcontrib><creatorcontrib>Lee, Hopin</creatorcontrib><creatorcontrib>Mansouri, Anita</creatorcontrib><creatorcontrib>Marian, Ioana R</creatorcontrib><creatorcontrib>Saccilotto, Ramon</creatorcontrib><creatorcontrib>Nury, Edris</creatorcontrib><creatorcontrib>Kasenda, Benjamin</creatorcontrib><creatorcontrib>Ojeda-Ruiz, Elena</creatorcontrib><creatorcontrib>Schandelmaier, Stefan</creatorcontrib><creatorcontrib>Tomonaga, Yuki</creatorcontrib><creatorcontrib>Amstutz, 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Dominik</creatorcontrib><creatorcontrib>Blümle, Anette</creatorcontrib><creatorcontrib>von Niederhäusern, Belinda</creatorcontrib><creatorcontrib>Hopewell, Sally</creatorcontrib><creatorcontrib>Odutayo, Ayodele</creatorcontrib><creatorcontrib>Briel, Matthias</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium 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UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><collection>PLoS Medicine</collection><jtitle>PLoS medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Speich, Benjamin</au><au>Gryaznov, Dmitry</au><au>Busse, Jason W</au><au>Gloy, Viktoria L</au><au>Lohner, Szimonetta</au><au>Klatte, Katharina</au><au>Taji Heravi, Ala</au><au>Ghosh, Nilabh</au><au>Lee, Hopin</au><au>Mansouri, Anita</au><au>Marian, Ioana R</au><au>Saccilotto, Ramon</au><au>Nury, Edris</au><au>Kasenda, Benjamin</au><au>Ojeda-Ruiz, Elena</au><au>Schandelmaier, Stefan</au><au>Tomonaga, Yuki</au><au>Amstutz, Alain</au><au>Pauli-Magnus, Christiane</au><au>Bischoff, Karin</au><au>Wollmann, Katharina</au><au>Rehner, Laura</au><au>Meerpohl, Joerg J</au><au>Nordmann, Alain</au><au>Wong, Jacqueline</au><au>Chow, Ngai</au><au>Hong, Patrick Jiho</au><au>Mc Cord-De Iaco, Kimberly</au><au>Sricharoenchai, Sirintip</au><au>Agarwal, Arnav</au><au>Schwenkglenks, Matthias</au><au>Hemkens, Lars G</au><au>von Elm, Erik</au><au>Copsey, Bethan</au><au>Griessbach, Alexandra N</au><au>Schönenberger, Christof</au><au>Mertz, Dominik</au><au>Blümle, Anette</au><au>von Niederhäusern, Belinda</au><au>Hopewell, Sally</au><au>Odutayo, Ayodele</au><au>Briel, Matthias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nonregistration, discontinuation, and nonpublication of randomized trials: A repeated metaresearch analysis</atitle><jtitle>PLoS medicine</jtitle><addtitle>PLoS Med</addtitle><date>2022-04-27</date><risdate>2022</risdate><volume>19</volume><issue>4</issue><spage>e1003980</spage><epage>e1003980</epage><pages>e1003980-e1003980</pages><issn>1549-1676</issn><issn>1549-1277</issn><eissn>1549-1676</eissn><abstract>We previously found that 25% of 1,017 randomized clinical trials (RCTs) approved between 2000 and 2003 were discontinued prematurely, and 44% remained unpublished at a median of 12 years follow-up. We aimed to assess a decade later (1) whether rates of completion and publication have increased; (2) the extent to which nonpublished RCTs can be identified in trial registries; and (3) the association between reporting quality of protocols and premature discontinuation or nonpublication of RCTs. We included 326 RCT protocols approved in 2012 by research ethics committees in Switzerland, the United Kingdom, Germany, and Canada in this metaresearch study. Pilot, feasibility, and phase 1 studies were excluded. We extracted trial characteristics from each study protocol and systematically searched for corresponding trial registration (if not reported in the protocol) and full text publications until February 2022. For trial registrations, we searched the (i) World Health Organization: International Clinical Trial Registry Platform (ICTRP); (ii) US National Library of Medicine (ClinicalTrials.gov); (iii) European Union Drug Regulating Authorities Clinical Trials Database (EUCTR); (iv) ISRCTN registry; and (v) Google. For full text publications, we searched PubMed, Google Scholar, and Scopus. We recorded whether RCTs were registered, discontinued (including reason for discontinuation), and published. The reporting quality of RCT protocols was assessed with the 33-item SPIRIT checklist. We used multivariable logistic regression to examine the association between the independent variables protocol reporting quality, planned sample size, type of control (placebo versus other), reporting of any recruitment projection, single-center versus multicenter trials, and industry versus investigator sponsoring, with the 2 dependent variables: (1) publication of RCT results; and (2) trial discontinuation due to poor recruitment. Of the 326 included trials, 19 (6%) were unregistered. Ninety-eight trials (30%) were discontinued prematurely, most often due to poor recruitment (37%; 36/98). One in 5 trials (21%; 70/326) remained unpublished at 10 years follow-up, and 21% of unpublished trials (15/70) were unregistered. Twenty-three of 147 investigator-sponsored trials (16%) reported their results in a trial registry in contrast to 150 of 179 industry-sponsored trials (84%). The median proportion of reported SPIRIT items in included RCT protocols was 69% (interquartile range 61% to 77%). We found no variables associated with trial discontinuation; however, lower reporting quality of trial protocols was associated with nonpublication (odds ratio, 0.71 for each 10% increment in the proportion of SPIRIT items met; 95% confidence interval, 0.55 to 0.92; p = 0.009). Study limitations include that the moderate sample size may have limited the ability of our regression models to identify significant associations. We have observed that rates of premature trial discontinuation have not changed in the past decade. Nonpublication of RCTs has declined but remains common; 21% of unpublished trials could not be identified in registries. Only 16% of investigator-sponsored trials reported results in a trial registry. Higher reporting quality of RCT protocols was associated with publication of results. Further efforts from all stakeholders are needed to improve efficiency and transparency of clinical research.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>35476675</pmid><doi>10.1371/journal.pmed.1003980</doi><orcidid>https://orcid.org/0000-0002-4438-4961</orcidid><orcidid>https://orcid.org/0000-0003-3726-1856</orcidid><orcidid>https://orcid.org/0000-0002-6292-4802</orcidid><orcidid>https://orcid.org/0000-0001-7853-4967</orcidid><orcidid>https://orcid.org/0000-0002-7583-8137</orcidid><orcidid>https://orcid.org/0000-0002-8429-0337</orcidid><orcidid>https://orcid.org/0000-0002-0692-8112</orcidid><orcidid>https://orcid.org/0000-0003-1716-993X</orcidid><orcidid>https://orcid.org/0000-0003-4337-1613</orcidid><orcidid>https://orcid.org/0000-0003-2877-1029</orcidid><orcidid>https://orcid.org/0000-0001-7217-1173</orcidid><orcidid>https://orcid.org/0000-0002-2361-6794</orcidid><orcidid>https://orcid.org/0000-0003-3752-1611</orcidid><orcidid>https://orcid.org/0000-0002-4620-7010</orcidid><orcidid>https://orcid.org/0000-0002-1333-5403</orcidid><orcidid>https://orcid.org/0000-0002-0931-7851</orcidid><orcidid>https://orcid.org/0000-0003-0110-8585</orcidid><orcidid>https://orcid.org/0000-0002-7500-1636</orcidid><orcidid>https://orcid.org/0000-0002-2070-5230</orcidid><orcidid>https://orcid.org/0000-0003-1710-5450</orcidid><orcidid>https://orcid.org/0000-0002-9856-3500</orcidid><orcidid>https://orcid.org/0000-0002-0178-8712</orcidid><orcidid>https://orcid.org/0000-0002-7412-0406</orcidid><orcidid>https://orcid.org/0000-0001-5098-0375</orcidid><orcidid>https://orcid.org/0000-0002-3444-1432</orcidid><orcidid>https://orcid.org/0000-0001-5692-0314</orcidid><orcidid>https://orcid.org/0000-0002-2147-3160</orcidid><orcidid>https://orcid.org/0000-0002-3301-8085</orcidid><orcidid>https://orcid.org/0000-0001-9783-6549</orcidid><oa>free_for_read</oa></addata></record>
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subjects Clinical trials
Data collection
Feasibility studies
Germany
Humans
Intervention
Management
Medical research
Medicine and Health Sciences
Medicine, Experimental
Methods
Odds Ratio
Patients
Randomized Controlled Trials as Topic
Registration
Registries
Regression analysis
Research and Analysis Methods
Research ethics
Research Personnel
Science Policy
Statistics
Variables
title Nonregistration, discontinuation, and nonpublication of randomized trials: A repeated metaresearch analysis
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