Nonregistration, discontinuation, and nonpublication of randomized trials

Standard

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

in: PLOS MED, Jahrgang 19, Nr. 4, e1003980, 04.2022.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Speich, B, Gryaznov, D, Busse, JW, Gloy, VL, Lohner, S, Klatte, K, Taji Heravi, A, Ghosh, N, Lee, H, Mansouri, A, Marian, IR, Saccilotto, R, Nury, OE, Kasenda, B, Ojeda-Ruiz, E, Schandelmaier, S, Tomonaga, Y, Amstutz, A, Pauli-Magnus, C, Bischoff, K, Wollmann, K, Rehner, L, Meerpohl, JJ, Nordmann, A, Wong, J, Chow, N, Hong, PJ, Mc Cord-De Iaco, K, Sricharoenchai, S, Agarwal, A, Schwenkglenks, M, Hemkens, LG, von Elm, E, Copsey, B, Griessbach, AN, Schönenberger, C, Mertz, D, Blümle, A, von Niederhäusern, B, Hopewell, S, Odutayo, A & Briel, M 2022, 'Nonregistration, discontinuation, and nonpublication of randomized trials: A repeated metaresearch analysis', PLOS MED, Jg. 19, Nr. 4, e1003980. https://doi.org/10.1371/journal.pmed.1003980

APA

Speich, B., Gryaznov, D., Busse, J. W., Gloy, V. L., Lohner, S., Klatte, K., Taji Heravi, A., Ghosh, N., Lee, H., Mansouri, A., Marian, I. R., Saccilotto, R., Nury, O. E., Kasenda, B., Ojeda-Ruiz, E., Schandelmaier, S., Tomonaga, Y., Amstutz, A., Pauli-Magnus, C., ... Briel, M. (2022). Nonregistration, discontinuation, and nonpublication of randomized trials: A repeated metaresearch analysis. PLOS MED, 19(4), [e1003980]. https://doi.org/10.1371/journal.pmed.1003980

Vancouver

Bibtex

@article{3ae90a3368c24b33a7f33b48ca1b6589,
title = "Nonregistration, discontinuation, and nonpublication of randomized trials: A repeated metaresearch analysis",
abstract = "BACKGROUND: 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.METHODS AND FINDINGS: 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.CONCLUSIONS: 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.",
keywords = "Germany, Humans, Odds Ratio, Randomized Controlled Trials as Topic, Registries, Research Personnel",
author = "Benjamin Speich and Dmitry Gryaznov and Busse, {Jason W} and Gloy, {Viktoria L} and Szimonetta Lohner and Katharina Klatte and {Taji Heravi}, Ala and Nilabh Ghosh and Hopin Lee and Anita Mansouri and Marian, {Ioana R} and Ramon Saccilotto and Nury, {Oshika Edris} and Benjamin Kasenda and Elena Ojeda-Ruiz and Stefan Schandelmaier and Yuki Tomonaga and Alain Amstutz and Christiane Pauli-Magnus and Karin Bischoff and Katharina Wollmann and Laura Rehner and Meerpohl, {Joerg J} and Alain Nordmann and Jacqueline Wong and Ngai Chow and Hong, {Patrick Jiho} and {Mc Cord-De Iaco}, Kimberly and Sirintip Sricharoenchai and Arnav Agarwal and Matthias Schwenkglenks and Hemkens, {Lars G} and {von Elm}, Erik and Bethan Copsey and Griessbach, {Alexandra N} and Christof Sch{\"o}nenberger and Dominik Mertz and Anette Bl{\"u}mle and {von Niederh{\"a}usern}, Belinda and Sally Hopewell and Ayodele Odutayo and Matthias Briel",
year = "2022",
month = apr,
doi = "10.1371/journal.pmed.1003980",
language = "English",
volume = "19",
journal = "PLOS MED",
issn = "1549-1277",
publisher = "Public Library of Science",
number = "4",

}

RIS

TY - JOUR

T1 - Nonregistration, discontinuation, and nonpublication of randomized trials

T2 - A repeated metaresearch analysis

AU - Speich, Benjamin

AU - Gryaznov, Dmitry

AU - Busse, Jason W

AU - Gloy, Viktoria L

AU - Lohner, Szimonetta

AU - Klatte, Katharina

AU - Taji Heravi, Ala

AU - Ghosh, Nilabh

AU - Lee, Hopin

AU - Mansouri, Anita

AU - Marian, Ioana R

AU - Saccilotto, Ramon

AU - Nury, Oshika Edris

AU - Kasenda, Benjamin

AU - Ojeda-Ruiz, Elena

AU - Schandelmaier, Stefan

AU - Tomonaga, Yuki

AU - Amstutz, Alain

AU - Pauli-Magnus, Christiane

AU - Bischoff, Karin

AU - Wollmann, Katharina

AU - Rehner, Laura

AU - Meerpohl, Joerg J

AU - Nordmann, Alain

AU - Wong, Jacqueline

AU - Chow, Ngai

AU - Hong, Patrick Jiho

AU - Mc Cord-De Iaco, Kimberly

AU - Sricharoenchai, Sirintip

AU - Agarwal, Arnav

AU - Schwenkglenks, Matthias

AU - Hemkens, Lars G

AU - von Elm, Erik

AU - Copsey, Bethan

AU - Griessbach, Alexandra N

AU - Schönenberger, Christof

AU - Mertz, Dominik

AU - Blümle, Anette

AU - von Niederhäusern, Belinda

AU - Hopewell, Sally

AU - Odutayo, Ayodele

AU - Briel, Matthias

PY - 2022/4

Y1 - 2022/4

N2 - BACKGROUND: 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.METHODS AND FINDINGS: 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.CONCLUSIONS: 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.

AB - BACKGROUND: 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.METHODS AND FINDINGS: 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.CONCLUSIONS: 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.

KW - Germany

KW - Humans

KW - Odds Ratio

KW - Randomized Controlled Trials as Topic

KW - Registries

KW - Research Personnel

U2 - 10.1371/journal.pmed.1003980

DO - 10.1371/journal.pmed.1003980

M3 - SCORING: Journal article

C2 - 35476675

VL - 19

JO - PLOS MED

JF - PLOS MED

SN - 1549-1277

IS - 4

M1 - e1003980

ER -