Is this clinical trial fully registered? A statement from the International Committee of Medical Journal Editors
CD De Angelis, JM Drazen, FA Frizelle, C Haug… - The Lancet, 2005 - thelancet.com
Comment of 20 items (table). The WHO-mandated items collectively address every key
requirement that we established in our September, 2004, editorial. The ICMJE supports the …
requirement that we established in our September, 2004, editorial. The ICMJE supports the …
Clinical trial registration: looking back and moving ahead
C Laine, R Horton, CD DeAngelis, JM Drazen… - The Lancet, 2007 - thelancet.com
Comment 1910 www. thelancet. com Vol 369 June 9, 2007 require registration, and the
registration of trial results. As is always the case, the ICMJE establishes policy only for the 12 …
registration of trial results. As is always the case, the ICMJE establishes policy only for the 12 …
WHO facilitates international collaboration in setting standards for clinical trial registration
Clinical trial registration has been a popular topic in the past 12 months. WHO, 1 the
pharmaceutical industry, 2 several national research institutions, 3 and independent …
pharmaceutical industry, 2 several national research institutions, 3 and independent …
[HTML][HTML] Trial registration at ClinicalTrials. gov between May and October 2005
DA Zarin, T Tse, NC Ide - New England Journal of Medicine, 2005 - Mass Medical Soc
Background Clinical trial registration allows interested parties to obtain information about
ongoing and completed trials, but there are few data indicating the quality of the information …
ongoing and completed trials, but there are few data indicating the quality of the information …
Clinical trial registration: transparency is the watchword
13 Intervention (s) Specific name of intervention (s) and comparator/control (s). Use
International Non-Proprietary Name if possible (not brand/trade names). For unregistered …
International Non-Proprietary Name if possible (not brand/trade names). For unregistered …
[PDF][PDF] International standards for clinical trial registries: the registration of all interventional trials is a scientific, ethical and moral responsibility
World Health Organization - 2018 - apps.who.int
The International Clinical Trials Registry Platform (ICTRP) is a global initiative that aims to
make information about all clinical trials involving human beings publicly available. It was …
make information about all clinical trials involving human beings publicly available. It was …
Under-reporting of clinical trials is unethical
G Antes, I Chalmers - The Lancet, 2003 - thelancet.com
For personal use. Only reproduce with permission from The Lancet Publishing Group.
component of ethical review, and ensure that patients are advised to withold their consent to …
component of ethical review, and ensure that patients are advised to withold their consent to …
Trial registration: a great idea switches from ignored to irresistible
D Rennie - Jama, 2004 - jamanetwork.com
IN A RECENT ARTICLE IN JAMA ON THE REGISTRATION OF clinical trials, 1 Dickersin and
I pointed out that, 30 years after the idea of registering trials had been proposed, 18 years …
I pointed out that, 30 years after the idea of registering trials had been proposed, 18 years …
Registering clinical trials
K Dickersin, D Rennie - Jama, 2003 - jamanetwork.com
That it is not possible to find information about all initiated clinical trials is of international
concern. This is a particular worry because scientists tend to publish their positive findings …
concern. This is a particular worry because scientists tend to publish their positive findings …
The evolution of trial registries and their use to assess the clinical trial enterprise
K Dickersin, D Rennie - Jama, 2012 - jamanetwork.com
THE ORIGINAL PURPOSE OF REGISTRIES OF CLINICAL trials was to reveal the existence
of all trials, pub-lished or not, to investigators and systematic reviewers. Trials left …
of all trials, pub-lished or not, to investigators and systematic reviewers. Trials left …