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1,017 randomized clinical trials (RCTs) approved between 2000 and 2003 were discontinued prematurely, and 44% remained unpublished at a median of 12 years follow-up.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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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1,017 randomized clinical trials (RCTs) approved between 2000 and 2003 were discontinued prematurely, and 44% remained unpublished at a median of 12 years follow-up.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 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, Matthias</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c764t-438c8575a3ada0b03728d6a27dbc81eff8f75668b738549f2b519fa4454df5ec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Clinical trials</topic><topic>Data collection</topic><topic>Feasibility studies</topic><topic>Germany</topic><topic>Humans</topic><topic>Intervention</topic><topic>Management</topic><topic>Medical research</topic><topic>Medicine and Health Sciences</topic><topic>Medicine, Experimental</topic><topic>Methods</topic><topic>Odds Ratio</topic><topic>Patients</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Registration</topic><topic>Registries</topic><topic>Regression analysis</topic><topic>Research and Analysis Methods</topic><topic>Research ethics</topic><topic>Research Personnel</topic><topic>Science 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 & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium 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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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source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Public Library of Science (PLoS) |
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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