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VERSION DATE APRIL 22, 2016TITLE: A comparison of early deployment of a video capsule (Endocapsule EC10: Olympus Tokyo. Japan) in the Emergency Department versus conventional workup of hematemesis
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01
Create a clear research question and hypothesis for the randomized controlled trial.
02
Design the trial protocol, including the study population, sample size, and randomization process.
03
Obtain ethical approval from relevant ethics committees or institutional review boards.
04
Recruit eligible participants and obtain informed consent from them.
05
Randomly assign participants to either the control group or the intervention group.
06
Implement the intervention or control condition according to the trial protocol.
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Collect data on outcome measures from both groups.
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Analyze the data using appropriate statistical methods.
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Interpret the results and draw conclusions based on the findings.
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Communicate the results through publication or presentation.

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Randomized controlled trials are typically used by researchers in the field of medicine and healthcare.
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Pharmaceutical companies often conduct randomized controlled trials to test the efficacy and safety of new drugs.
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Government health agencies may require randomized controlled trials to support the approval of healthcare interventions.
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Doctors and healthcare professionals may use the results of randomized controlled trials to inform their clinical practice.
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Patients and the general public can benefit from randomized controlled trials as they provide evidence-based guidance on treatments and interventions.

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