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itopride mosapride The study of itopride and mosapride usage in OutPatient Department at Phyathai Sriracha Hospital . . .
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A randomised double-blind comparative study is a research design in which participants are randomly assigned to either a treatment group or a control group, and neither the participants nor the researchers know which group the participants belong to. This method helps to eliminate bias in the results.
Researchers planning to conduct clinical trials or studies involving drug treatments and interventions typically are required to file a randomised double-blind comparative study.
To fill out a randomised double-blind comparative study, researchers must provide detailed information about the study design, participant demographics, methods of randomization, blinding procedures, and data analysis plans. This often includes completing specific forms required by regulatory bodies.
The purpose of a randomised double-blind comparative study is to evaluate the efficacy and safety of a treatment by comparing it against a control group while minimizing bias and ensuring that the treatment effects are attributed to the intervention itself.
Information that must be reported includes the study design, sample size, participant demographics, inclusion and exclusion criteria, methods of randomization and blinding, statistical analysis plan, and results with interpretations.
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