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TITLE PAGE TITLE: Acetic acid chromoendoscopy in Barrett's esophagus surveillance is superior to the standardized random biopsy protocol in detecting neoplasm: A prospective randomized trial. Coordinating
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Determine the objectives and hypothesis of the investigator-initiated study.
02
Develop a study protocol outlining the study design, population, and data collection methods.
03
Obtain any necessary ethical approvals or institutional review board (IRB) clearance.
04
Recruit participants that meet the study criteria and obtain informed consent.
05
Collect and record the required study data according to the protocol.
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Analyze the collected data using appropriate statistical methods.
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Interpret the results and draw conclusions based on the study findings.
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Who needs investigator initiated study data?

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Researchers conducting clinical or observational studies.
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Healthcare organizations or institutions interested in studying the effectiveness or safety of a particular intervention.
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Government agencies or regulatory bodies overseeing clinical trials and research.
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Pharmaceutical or biotechnology companies exploring new indications for their products.
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Investigator initiated study data refers to research studies that are proposed, conducted, and funded by researchers or institutions.
Researchers or institutions conducting investigator initiated studies are required to file the data.
Investigators can fill out the data by providing relevant information about the study design, methods, results, and any publications.
The purpose of investigator initiated study data is to provide transparency and share research findings with the scientific community.
Investigators must report details about the study design, methods, results, funding sources, and any conflicts of interest.
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