পদ্ধতির তুলনা করুন

	ক্লিনিক্যাল ট্রায়াল রেজিস্ট্রেশন	Research with Vulnerable Populations
ক্ষেত্র	গবেষণা নৈতিকতা	গবেষণা নৈতিকতা
পরিবার	Process / pipeline	Process / pipeline
উদ্ভবের বছর	2005	1979
প্রবর্তক	World Health Organization; International Committee of Medical Journal Editors	U.S. Department of Health and Human Services; World Health Organization; International research ethics community
ধরন	Requirement	Guideline
মৌলিক উৎস	World Health Organization. (2005). Ensuring that Studies Are Prospectively Registered. International Clinical Trials Registry Platform (ICTRP) Statement.	U.S. Department of Health and Human Services. (2018). Protection of Human Subjects. Code of Federal Regulations Title 45, Part 46, Subparts B, C, D.
অপর নাম	trial registration, prospective registration, ClinicalTrials.gov, trial registry	vulnerable subjects, special populations, vulnerable groups, additional protections
সম্পর্কিত	5	5
সারসংক্ষেপ	Clinical trial registration is the prospective documentation of a trial's key information (hypothesis, design, population, outcomes) in a public registry before enrollment begins or results are known. In 2005, the World Health Organization established the requirement that all clinical trials be registered in an internationally recognized registry before participant enrollment. The International Committee of Medical Journal Editors (ICMJE) made registration a condition for publication in major medical journals in 2005, updated in 2015. Primary registries include ClinicalTrials.gov (U.S.), ISRCTN (UK), EudraCT (EU), and others operating under WHO oversight. Registration serves to prevent selective outcome reporting, reduce publication bias, and enhance research transparency.	Vulnerable populations are groups with limited capacity to protect themselves due to age, cognitive ability, institutional dependency, or social circumstances. Regulatory frameworks in the U.S. (45 CFR 46 Subparts B, C, D) and internationally identify specific vulnerable populations—children, prisoners, pregnant women, cognitively impaired individuals—and mandate additional ethical protections beyond standard informed consent. These protections include obtaining informed consent from surrogate decision-makers (parents, guardians), additional assurances of minimal risk, and enhanced monitoring for safety. Research ethics committees apply heightened scrutiny to studies involving vulnerable populations and may deny approval if special protections are inadequate.