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COVER PAGE PROTOCOL November 3, 2017, Rev. 1.0 NCT03178942 A Randomized, DoubleClick, ParallelDesign, Multiple Site Study to Evaluate the Therapeutic Equivalence of Permethrin Cream, 5% (En cube Ethical)
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How to fill out a randomized double-blind parallel-design

01
To fill out a randomized double-blind parallel-design, follow these steps:
02
Determine the objectives and research questions of your study.
03
Design the study protocol, including the selection criteria for participants, randomization procedures, and blinding methods.
04
Identify a suitable sample size based on statistical power calculations.
05
Recruit eligible participants and obtain their informed consent.
06
Randomly assign participants to either the intervention or control group.
07
Implement the intervention or treatment in the intervention group and ensure the control group receives a placebo or standard treatment.
08
Collect data on the outcomes of interest while ensuring blinding is maintained.
09
Analyze the data using appropriate statistical methods.
10
Interpret the results and draw conclusions based on the findings of the study.
11
Report the study design, methods, results, and conclusions following the recommended guidelines for scientific publications.

Who needs a randomized double-blind parallel-design?

01
A randomized double-blind parallel-design is needed in various research contexts, including but not limited to:
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- Clinical trials evaluating new drugs or treatments
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- Comparative effectiveness studies
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- Research investigating the efficacy of interventions
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- Experimental studies in psychology or social sciences
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- Studies aiming to reduce biases and increase scientific rigor in research
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A randomized double-blind parallel-design is a research study in which participants are randomly assigned to different treatment groups, neither the participants nor the researchers know which treatment each participant is receiving, and the study involves comparing two or more treatments at the same time.
Researchers conducting clinical trials or research studies that involve comparing different treatments are required to file a randomized double-blind parallel-design.
To fill out a randomized double-blind parallel-design, researchers need to carefully plan the study design, randomize participants to different treatment groups, ensure blinding of participants and researchers, and collect and analyze data according to the study protocol.
The purpose of a randomized double-blind parallel-design is to minimize biases and ensure that the results of the study are reliable and unbiased by eliminating the influence of both participants and researchers on the outcomes.
A randomized double-blind parallel-design must report details of the study design, randomization process, blinding procedures, treatment groups, outcomes measured, analysis methods, and potential conflicts of interest.
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