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A single center, doubleblinded randomized placebocontrolled trial to evaluate surgical scars after treatment with fractional carbon dioxide rejuvenation laser therapyNCT02985151 Approved: 06 May 2017SLU
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Obtain approval from an ethics committee or institutional review board.
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Randomly assign participants to either the control group or the experimental group.
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Ensure that neither the participants nor the researchers know which group each participant is assigned to.
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Collect data on the outcomes of interest in a way that does not reveal the group assignments.
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Analyze the data without knowing the group assignments to minimize bias.

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A single center double-blinded study is a type of clinical trial where both the participants and the researchers do not know which individuals are receiving the treatment and which are receiving a placebo, and it is conducted at a single location.
Researchers conducting the clinical trial, along with their institutions, are typically required to file a single center double-blinded study with the appropriate regulatory bodies.
To fill out a single center double-blinded form, researchers must provide details about the study design, participant information, treatment protocols, and data collection methods, as well as any necessary approvals.
The purpose of a single center double-blinded study is to eliminate bias in clinical trials by ensuring that neither the participants nor the researchers influence the results.
Information that must be reported includes study objectives, methodology, participant demographics, treatment details, outcome measures, and results.
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