DOI: 10.1503/cmaj. 1041299 pared the contents of 102 trial protocols approved by the
scientific ethics committees for Copenhagen and Frederiksberg, Denmark, during 1994 and …

Abandoned Trials has been called RIAT. Recent litigation and new freedom of information
rules in Europe have facilitated the ability of investigators to access clinical study reports …

The official position of the Society for Clinical Trials is to support legislation in the United
States and internationally that mandates registration of all controlled clinicals trials at or …

Background Randomised clinical trials are key to advancing medical knowledge and to
enhancing patient care, but major barriers to their conduct exist. The present paper presents …

Transparency of clinical trials is one of the main objectives that any responsible trialist,
sponsor or funder should meet. This should include all relevant aspects related to the …

Randomised controlled trials are the gold standard for testing the efficacy and safety of
health interventions, especially medications, and researchers in the UK are required to gain …

There have been a growing number of calls for public registration and results reporting of
clinical trials as a method for addressing scientific and ethical concerns.'ClinicalTrials. gov …

• The Canadian Institutes of Health Research (CIHR), preferably with the creation of a new
agency or vice-presidential position for human applied research, should increase funding for …

Reporting of informed consent, standard of care and post-trial obligations in global
randomized intervention trials: A systematic survey of registered trials. Emma RM Cohen …

In the decade following the journal editors' trial registration policy, a global trial reporting
system (TRS) has arisen to supplement journal publication by increasing the transparency …