Capsaicin 8% patch repeat treatment plus standard of care (SOC) versus SOC alone in painful diabetic peripheral neuropathy: a randomised, 52-week, open-label, safety study

This 52-week study evaluated the long-term safety and tolerability of capsaicin 8% w/w (179 mg) patch repeat treatment plus standard of care (SOC) versus SOC alone in painful diabetic peripheral neuropathy (PDPN). Phase 3, multinational, open-label, randomised, controlled, 52-week safety study, cond...

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Veröffentlicht in:BMC neurology 2016-12, Vol.16 (1), p.251-251, Article 251
Hauptverfasser: Vinik, Aaron I, Perrot, Serge, Vinik, Etta J, Pazdera, Ladislav, Jacobs, Hélène, Stoker, Malcolm, Long, Stephen K, Snijder, Robert J, van der Stoep, Marjolijne, Ortega, Enrique, Katz, Nathaniel
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container_end_page 251
container_issue 1
container_start_page 251
container_title BMC neurology
container_volume 16
creator Vinik, Aaron I
Perrot, Serge
Vinik, Etta J
Pazdera, Ladislav
Jacobs, Hélène
Stoker, Malcolm
Long, Stephen K
Snijder, Robert J
van der Stoep, Marjolijne
Ortega, Enrique
Katz, Nathaniel
description This 52-week study evaluated the long-term safety and tolerability of capsaicin 8% w/w (179 mg) patch repeat treatment plus standard of care (SOC) versus SOC alone in painful diabetic peripheral neuropathy (PDPN). Phase 3, multinational, open-label, randomised, controlled, 52-week safety study, conducted in Europe. Patients were randomised to capsaicin 8% patch repeat treatment (30 or 60 min; 1-7 treatments with ≥ 8-week intervals) to painful areas of the feet plus SOC, or SOC alone. The primary objective was the safety of capsaicin 8% patch repeat treatment (30 min and 60 min applications) plus SOC versus SOC alone over 52 weeks, assessed by changes in Norfolk Quality of Life-Diabetic Neuropathy (QOL-DN) total score from baseline to end of study (EOS). Secondary safety endpoints included Utah Early Neuropathy Scale (UENS) assessments and standardised testing of sensory perception and reflex function. Overall, 468 patients were randomised (30 min plus SOC, n = 156; 60 min plus SOC, n = 157; SOC alone, n = 155). By EoS, mean changes in Norfolk QOL-DN total score from baseline [estimated mean difference versus SOC alone; 90% CI for difference] were: 30 min plus SOC, -27.6% [-20.9; -31.7, -10.1]; 60 min plus SOC, -32.8% [-26.1; -36.8, -15.4]; SOC alone, -6.7%. Mean changes [difference versus SOC alone] in UENS total score by EoS versus baseline were: 30 min plus SOC, -2.1 [-0.9; -1.8, 0.1]; 60 min plus SOC, -3.0 [-1.7; -2.7, -0.8]; SOC alone, -1.2. No detrimental deterioration was observed in any of the Norfolk or UENS subscales by EoS with capsaicin. Also, no worsening in sensory perception testing of sharp, warm, cold and vibration stimuli was found with capsaicin by EoS. Capsaicin treatment was well tolerated and the most frequent treatment-emergent adverse events were application site pain (30 min, 28.2%; 60 min, 29.3%), burning sensation (30 min, 9.0%; 60 min, 9.6%) and application site erythema (30 min, 7.7%; 60 min, 8.9%). In patients with PDPN, capsaicin 8% patch repeat treatment plus SOC over 52 weeks was well tolerated with no negative functional or neurological effects compared with SOC alone. ClinicalTrials.gov registration: NCT01478607 . Date of registration November 21, 2011; retrospectively registered.
doi_str_mv 10.1186/s12883-016-0752-7
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Phase 3, multinational, open-label, randomised, controlled, 52-week safety study, conducted in Europe. Patients were randomised to capsaicin 8% patch repeat treatment (30 or 60 min; 1-7 treatments with ≥ 8-week intervals) to painful areas of the feet plus SOC, or SOC alone. The primary objective was the safety of capsaicin 8% patch repeat treatment (30 min and 60 min applications) plus SOC versus SOC alone over 52 weeks, assessed by changes in Norfolk Quality of Life-Diabetic Neuropathy (QOL-DN) total score from baseline to end of study (EOS). Secondary safety endpoints included Utah Early Neuropathy Scale (UENS) assessments and standardised testing of sensory perception and reflex function. Overall, 468 patients were randomised (30 min plus SOC, n = 156; 60 min plus SOC, n = 157; SOC alone, n = 155). By EoS, mean changes in Norfolk QOL-DN total score from baseline [estimated mean difference versus SOC alone; 90% CI for difference] were: 30 min plus SOC, -27.6% [-20.9; -31.7, -10.1]; 60 min plus SOC, -32.8% [-26.1; -36.8, -15.4]; SOC alone, -6.7%. Mean changes [difference versus SOC alone] in UENS total score by EoS versus baseline were: 30 min plus SOC, -2.1 [-0.9; -1.8, 0.1]; 60 min plus SOC, -3.0 [-1.7; -2.7, -0.8]; SOC alone, -1.2. No detrimental deterioration was observed in any of the Norfolk or UENS subscales by EoS with capsaicin. Also, no worsening in sensory perception testing of sharp, warm, cold and vibration stimuli was found with capsaicin by EoS. Capsaicin treatment was well tolerated and the most frequent treatment-emergent adverse events were application site pain (30 min, 28.2%; 60 min, 29.3%), burning sensation (30 min, 9.0%; 60 min, 9.6%) and application site erythema (30 min, 7.7%; 60 min, 8.9%). In patients with PDPN, capsaicin 8% patch repeat treatment plus SOC over 52 weeks was well tolerated with no negative functional or neurological effects compared with SOC alone. ClinicalTrials.gov registration: NCT01478607 . Date of registration November 21, 2011; retrospectively registered.</description><identifier>ISSN: 1471-2377</identifier><identifier>EISSN: 1471-2377</identifier><identifier>DOI: 10.1186/s12883-016-0752-7</identifier><identifier>PMID: 27919222</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Administration, Cutaneous ; Adult ; Aged ; Capsaicin ; Capsaicin - administration &amp; dosage ; Capsaicin - adverse effects ; Care and treatment ; Comparative analysis ; Diabetic Neuropathies - complications ; Diabetic Neuropathies - drug therapy ; Female ; Humans ; Male ; Management ; Medical care ; Middle Aged ; Neuralgia - drug therapy ; Neuralgia - etiology ; Outcome Assessment (Health Care) ; Polyneuropathies ; Sensory System Agents - administration &amp; dosage ; Sensory System Agents - adverse effects ; Standard of Care</subject><ispartof>BMC neurology, 2016-12, Vol.16 (1), p.251-251, Article 251</ispartof><rights>COPYRIGHT 2016 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2016</rights><rights>The Author(s). 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c520t-dd0658ea86af0726f8b586697c6ae2cd6d897fa2556d192698d41c643d8baed53</citedby><cites>FETCH-LOGICAL-c520t-dd0658ea86af0726f8b586697c6ae2cd6d897fa2556d192698d41c643d8baed53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5139122/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5139122/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27919222$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vinik, Aaron I</creatorcontrib><creatorcontrib>Perrot, Serge</creatorcontrib><creatorcontrib>Vinik, Etta J</creatorcontrib><creatorcontrib>Pazdera, Ladislav</creatorcontrib><creatorcontrib>Jacobs, Hélène</creatorcontrib><creatorcontrib>Stoker, Malcolm</creatorcontrib><creatorcontrib>Long, Stephen K</creatorcontrib><creatorcontrib>Snijder, Robert J</creatorcontrib><creatorcontrib>van der Stoep, Marjolijne</creatorcontrib><creatorcontrib>Ortega, Enrique</creatorcontrib><creatorcontrib>Katz, Nathaniel</creatorcontrib><title>Capsaicin 8% patch repeat treatment plus standard of care (SOC) versus SOC alone in painful diabetic peripheral neuropathy: a randomised, 52-week, open-label, safety study</title><title>BMC neurology</title><addtitle>BMC Neurol</addtitle><description>This 52-week study evaluated the long-term safety and tolerability of capsaicin 8% w/w (179 mg) patch repeat treatment plus standard of care (SOC) versus SOC alone in painful diabetic peripheral neuropathy (PDPN). Phase 3, multinational, open-label, randomised, controlled, 52-week safety study, conducted in Europe. Patients were randomised to capsaicin 8% patch repeat treatment (30 or 60 min; 1-7 treatments with ≥ 8-week intervals) to painful areas of the feet plus SOC, or SOC alone. The primary objective was the safety of capsaicin 8% patch repeat treatment (30 min and 60 min applications) plus SOC versus SOC alone over 52 weeks, assessed by changes in Norfolk Quality of Life-Diabetic Neuropathy (QOL-DN) total score from baseline to end of study (EOS). Secondary safety endpoints included Utah Early Neuropathy Scale (UENS) assessments and standardised testing of sensory perception and reflex function. Overall, 468 patients were randomised (30 min plus SOC, n = 156; 60 min plus SOC, n = 157; SOC alone, n = 155). By EoS, mean changes in Norfolk QOL-DN total score from baseline [estimated mean difference versus SOC alone; 90% CI for difference] were: 30 min plus SOC, -27.6% [-20.9; -31.7, -10.1]; 60 min plus SOC, -32.8% [-26.1; -36.8, -15.4]; SOC alone, -6.7%. Mean changes [difference versus SOC alone] in UENS total score by EoS versus baseline were: 30 min plus SOC, -2.1 [-0.9; -1.8, 0.1]; 60 min plus SOC, -3.0 [-1.7; -2.7, -0.8]; SOC alone, -1.2. No detrimental deterioration was observed in any of the Norfolk or UENS subscales by EoS with capsaicin. Also, no worsening in sensory perception testing of sharp, warm, cold and vibration stimuli was found with capsaicin by EoS. Capsaicin treatment was well tolerated and the most frequent treatment-emergent adverse events were application site pain (30 min, 28.2%; 60 min, 29.3%), burning sensation (30 min, 9.0%; 60 min, 9.6%) and application site erythema (30 min, 7.7%; 60 min, 8.9%). In patients with PDPN, capsaicin 8% patch repeat treatment plus SOC over 52 weeks was well tolerated with no negative functional or neurological effects compared with SOC alone. ClinicalTrials.gov registration: NCT01478607 . Date of registration November 21, 2011; retrospectively registered.</description><subject>Administration, Cutaneous</subject><subject>Adult</subject><subject>Aged</subject><subject>Capsaicin</subject><subject>Capsaicin - administration &amp; dosage</subject><subject>Capsaicin - adverse effects</subject><subject>Care and treatment</subject><subject>Comparative analysis</subject><subject>Diabetic Neuropathies - complications</subject><subject>Diabetic Neuropathies - drug therapy</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Management</subject><subject>Medical care</subject><subject>Middle Aged</subject><subject>Neuralgia - drug therapy</subject><subject>Neuralgia - etiology</subject><subject>Outcome Assessment (Health Care)</subject><subject>Polyneuropathies</subject><subject>Sensory System Agents - administration &amp; dosage</subject><subject>Sensory System Agents - adverse effects</subject><subject>Standard of Care</subject><issn>1471-2377</issn><issn>1471-2377</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNptUl1rFDEUHUSxtfoDfJGACBV26iQz-RgfhLL4BYU-qM_hbnKnmzo7GZOZyv6m_sneZWttRQLJJfecc3NvTlG85NUJ50a9y1wYU5cVV2WlpSj1o-KQN5qXotb68b34oHiW82VVcW0a_rQ4ELrlrRDisLhewpghuDAw84aNMLk1SzgiTGxKtG9wmNjYz5nlCQYPybPYMQcJ2fG38-VbdoUpU5ZiBn0ckJHSCGHo5p75ACucgmMjpjCuMUHPBpxTpDrr7XsGLJFm3ISMfsGogd-IPxcsjjiUPVH7BcvQ4bSl4rPfPi-edNBnfHF7HhU_Pn38vvxSnp1__ro8PSudFNVUel8paRCMgq7SQnVmJY1SrXYKUDivvGl1B0JK5WkKqjW-4U41tTcrQC_ro-LDXnecVxv0jkZAL7djChtIWxsh2IeZIaztRbyyktctF4IEjm8FUvw1Y54steiw72HAOGfLTaNqpejPCPr6H-hlnNNA7RFKNkpqreu_qAvo0dJwI9V1O1F72mhhlDBihzr5D4qWx01w9DddoPsHBL4nuBRzTtjd9cgru3OY3TvMksPszmFWE-fV_eHcMf5Yqr4Bit_MQQ</recordid><startdate>20161206</startdate><enddate>20161206</enddate><creator>Vinik, Aaron I</creator><creator>Perrot, Serge</creator><creator>Vinik, Etta J</creator><creator>Pazdera, Ladislav</creator><creator>Jacobs, Hélène</creator><creator>Stoker, Malcolm</creator><creator>Long, Stephen K</creator><creator>Snijder, Robert J</creator><creator>van der Stoep, Marjolijne</creator><creator>Ortega, Enrique</creator><creator>Katz, Nathaniel</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20161206</creationdate><title>Capsaicin 8% patch repeat treatment plus standard of care (SOC) versus SOC alone in painful diabetic peripheral neuropathy: a randomised, 52-week, open-label, safety study</title><author>Vinik, Aaron I ; Perrot, Serge ; Vinik, Etta J ; Pazdera, Ladislav ; Jacobs, Hélène ; Stoker, Malcolm ; Long, Stephen K ; Snijder, Robert J ; van der Stoep, Marjolijne ; Ortega, Enrique ; Katz, Nathaniel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c520t-dd0658ea86af0726f8b586697c6ae2cd6d897fa2556d192698d41c643d8baed53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Administration, Cutaneous</topic><topic>Adult</topic><topic>Aged</topic><topic>Capsaicin</topic><topic>Capsaicin - administration &amp; dosage</topic><topic>Capsaicin - adverse effects</topic><topic>Care and treatment</topic><topic>Comparative analysis</topic><topic>Diabetic Neuropathies - complications</topic><topic>Diabetic Neuropathies - drug therapy</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Management</topic><topic>Medical care</topic><topic>Middle Aged</topic><topic>Neuralgia - drug therapy</topic><topic>Neuralgia - etiology</topic><topic>Outcome Assessment (Health Care)</topic><topic>Polyneuropathies</topic><topic>Sensory System Agents - administration &amp; 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Phase 3, multinational, open-label, randomised, controlled, 52-week safety study, conducted in Europe. Patients were randomised to capsaicin 8% patch repeat treatment (30 or 60 min; 1-7 treatments with ≥ 8-week intervals) to painful areas of the feet plus SOC, or SOC alone. The primary objective was the safety of capsaicin 8% patch repeat treatment (30 min and 60 min applications) plus SOC versus SOC alone over 52 weeks, assessed by changes in Norfolk Quality of Life-Diabetic Neuropathy (QOL-DN) total score from baseline to end of study (EOS). Secondary safety endpoints included Utah Early Neuropathy Scale (UENS) assessments and standardised testing of sensory perception and reflex function. Overall, 468 patients were randomised (30 min plus SOC, n = 156; 60 min plus SOC, n = 157; SOC alone, n = 155). By EoS, mean changes in Norfolk QOL-DN total score from baseline [estimated mean difference versus SOC alone; 90% CI for difference] were: 30 min plus SOC, -27.6% [-20.9; -31.7, -10.1]; 60 min plus SOC, -32.8% [-26.1; -36.8, -15.4]; SOC alone, -6.7%. Mean changes [difference versus SOC alone] in UENS total score by EoS versus baseline were: 30 min plus SOC, -2.1 [-0.9; -1.8, 0.1]; 60 min plus SOC, -3.0 [-1.7; -2.7, -0.8]; SOC alone, -1.2. No detrimental deterioration was observed in any of the Norfolk or UENS subscales by EoS with capsaicin. Also, no worsening in sensory perception testing of sharp, warm, cold and vibration stimuli was found with capsaicin by EoS. Capsaicin treatment was well tolerated and the most frequent treatment-emergent adverse events were application site pain (30 min, 28.2%; 60 min, 29.3%), burning sensation (30 min, 9.0%; 60 min, 9.6%) and application site erythema (30 min, 7.7%; 60 min, 8.9%). In patients with PDPN, capsaicin 8% patch repeat treatment plus SOC over 52 weeks was well tolerated with no negative functional or neurological effects compared with SOC alone. ClinicalTrials.gov registration: NCT01478607 . Date of registration November 21, 2011; retrospectively registered.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>27919222</pmid><doi>10.1186/s12883-016-0752-7</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects Administration, Cutaneous
Adult
Aged
Capsaicin
Capsaicin - administration & dosage
Capsaicin - adverse effects
Care and treatment
Comparative analysis
Diabetic Neuropathies - complications
Diabetic Neuropathies - drug therapy
Female
Humans
Male
Management
Medical care
Middle Aged
Neuralgia - drug therapy
Neuralgia - etiology
Outcome Assessment (Health Care)
Polyneuropathies
Sensory System Agents - administration & dosage
Sensory System Agents - adverse effects
Standard of Care
title Capsaicin 8% patch repeat treatment plus standard of care (SOC) versus SOC alone in painful diabetic peripheral neuropathy: a randomised, 52-week, open-label, safety study
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T19%3A50%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Capsaicin%208%25%20patch%20repeat%20treatment%20plus%20standard%20of%20care%20(SOC)%20versus%20SOC%20alone%20in%20painful%20diabetic%20peripheral%20neuropathy:%20a%20randomised,%2052-week,%20open-label,%20safety%20study&rft.jtitle=BMC%20neurology&rft.au=Vinik,%20Aaron%20I&rft.date=2016-12-06&rft.volume=16&rft.issue=1&rft.spage=251&rft.epage=251&rft.pages=251-251&rft.artnum=251&rft.issn=1471-2377&rft.eissn=1471-2377&rft_id=info:doi/10.1186/s12883-016-0752-7&rft_dat=%3Cgale_pubme%3EA472862823%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1854657773&rft_id=info:pmid/27919222&rft_galeid=A472862823&rfr_iscdi=true