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editorial
. 2006 May 6;332(7549):1086–1089. doi: 10.1136/bmj.332.7549.1086

Table 1.

Benefits of access to trial protocols: who, when, and why

Who When Why
Study participants
Before enrolment
Informed consent
Research ethics committees
Before enrolment
Ethical review and oversight from trial inception through to reporting
Funding agencies
Before enrolment
Scientific review and oversight from trial inception through to reporting
Systematic reviewers
After trial inception
Awareness of ongoing, unpublished, and published studies; oversight of accurate trial reporting in publications; detailed quality assessment
External reviewers
After trial inception
Monitoring of ongoing trials and dissemination of results; oversight of accurate reporting in publications; detailed quality assessment
Journal editors and peer reviewers
Before publication
Oversight of accurate reporting in submitted publications; detailed quality assessment
Health regulatory agencies Before regulatory approval Oversight of accurate reporting of submitted trial data; detailed quality assessment