Literature DB >> 24052678

Use of data from registered clinical trials to identify gaps in health research and development.

Roderik F Viergever1, Robert F Terry, Ghassan Karam.   

Abstract

OBJECTIVE: To explore what can be learnt about the current composition of the "global landscape" of health research and development (R&D) from data on the World Health Organization's International Clinical Trials Registry Platform (ICTRP).
METHODS: A random 5% sample of the records of clinical trials that were registered as interventional and actively recruiting was taken from the ICTRP database.
FINDINGS: Overall, 2381 records of trials were investigated. Analysis of these records indicated that, for every million disability-adjusted life years (DALYs) caused by communicable, maternal, perinatal and nutritional conditions, by noncommunicable diseases, or by injuries, the ICTRP database contained an estimated 7.4, 52.4 and 6.0 trials in which these causes of burden of disease were being investigated, respectively. For every million DALYs in high-income, upper-middle-income, lower-middle-income and low-income countries, an estimated 292.7, 13.4, 3.0 and 0.8 registered trials, respectively, were recruiting in such countries.
CONCLUSION: The ICTRP constitutes a valuable resource for assessing the global distribution of clinical trials and for informing policy development for health R&D. Populations in lower-income countries receive much less attention, in terms of clinical trial research, than populations in higher-income countries.

Entities:  

Mesh:

Year:  2013        PMID: 24052678      PMCID: PMC3777147          DOI: 10.2471/BLT.12.114454

Source DB:  PubMed          Journal:  Bull World Health Organ        ISSN: 0042-9686            Impact factor:   9.408


  31 in total

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4.  Transparency for clinical trials--the TEST Act.

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5.  Pediatric versus adult drug trials for conditions with high pediatric disease burden.

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6.  The ClinicalTrials.gov results database--update and key issues.

Authors:  Deborah A Zarin; Tony Tse; Rebecca J Williams; Robert M Califf; Nicholas C Ide
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8.  The quality of registration of clinical trials.

Authors:  Roderik F Viergever; Davina Ghersi
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9.  Pharmacokinetic research in children: an analysis of registered records of clinical trials.

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  13 in total

Review 1.  The evolution in registration of clinical trials: a chronicle of the historical calls and current initiatives promoting transparency.

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3.  Poverty-related and neglected diseases - an economic and epidemiological analysis of poverty relatedness and neglect in research and development.

Authors:  Peter von Philipsborn; Fridolin Steinbeis; Max E Bender; Sadie Regmi; Peter Tinnemann
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4.  The mismatch between the health research and development (R&D) that is needed and the R&D that is undertaken: an overview of the problem, the causes, and solutions.

Authors:  Roderik F Viergever
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5.  Why Most Clinical Research Is Not Useful.

Authors:  John P A Ioannidis
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6.  Automatic classification of registered clinical trials towards the Global Burden of Diseases taxonomy of diseases and injuries.

Authors:  Ignacio Atal; Jean-David Zeitoun; Aurélie Névéol; Philippe Ravaud; Raphaël Porcher; Ludovic Trinquart
Journal:  BMC Bioinformatics       Date:  2016-09-22       Impact factor: 3.169

7.  Trends in global clinical trial registration: an analysis of numbers of registered clinical trials in different parts of the world from 2004 to 2013.

Authors:  Roderik F Viergever; Keyang Li
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8.  Differential Globalization of Industry- and Non-Industry-Sponsored Clinical Trials.

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9.  The quality of registration of clinical trials: still a problem.

Authors:  Roderik F Viergever; Ghassan Karam; Andreas Reis; Davina Ghersi
Journal:  PLoS One       Date:  2014-01-10       Impact factor: 3.240

10.  A comparison between health research output and burden of disease in Arab countries: evidence from Palestine.

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Journal:  Health Res Policy Syst       Date:  2018-03-15
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