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APPENDIX 4: DATA ABSTRACTION FORMS a) Clinical Review Study Ref ID Author Publication year Country FundingStudy type Study design Setting Total sample size Number of eligible participants Number of
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Randomized clinical trials (RCTs) are scientific studies designed to test the efficacy and safety of new medical interventions, such as drugs, treatments, or procedures, by randomly assigning participants to different groups to compare outcomes.
Researchers or organizations conducting clinical trials involving human participants are required to register and file their trials to ensure transparency and comply with regulatory standards.
To fill out the registration for a randomized clinical trial, researchers need to provide detailed information about the study's purpose, design, methodology, participant criteria, and outcome measures, often within a designated online registry.
The purpose of randomized clinical trials is to determine the effectiveness and safety of a new intervention by minimizing bias and ensuring that the results are based on objective evidence.
Key information that must be reported includes the trial's objectives, methodology, statistical analysis plan, participant demographics, inclusion and exclusion criteria, and the planned outcomes.
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