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MASTER THESIS Awarding the academic title of Master of Medicine (M Med) Medical Faculty, University of Bern Postoperative Pain in Tourniquet Induced IschemiaReperfusion Injury in Total Knee Arthroplasty
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01
Identify the study title and objectives.
02
Document the study design and methodology.
03
Describe the inclusion and exclusion criteria for participants.
04
Outline the study procedures and schedule.
05
Detail the data collection and analysis methods.
06
Address ethical considerations and participant confidentiality.
07
Include any potential risks and benefits of the study.
08
Obtain approval from the appropriate ethics committee.
09
Update the study protocol as needed throughout the research process.

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Researchers conducting clinical trials or observational studies.
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Institutional review boards reviewing research proposals.
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Regulatory agencies evaluating the safety and efficacy of new interventions.
05
Research sponsors overseeing the progress of a study.
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A study protocol is a detailed plan that outlines the objectives, design, methodology, statistical considerations, and organization of a research study.
Researchers or institutions conducting the study are typically required to file the study protocol with the relevant regulatory or ethics bodies.
To fill out a study protocol, researchers should follow specific guidelines provided by the regulatory body, ensuring they include sections such as objectives, methodology, and ethical considerations.
The purpose of a study protocol is to provide a clear framework for conducting research, ensuring that it is systematic, ethical, and reproducible.
Information that must be reported includes study objectives, design, methodology, participant criteria, data collection methods, and ethical considerations.
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