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Official Title:A Randomized, Placebo controlled Trial to Evaluate the Long term (i.e., Maintenance) Efficacy of Oral in the Treatment of Pediatric Subjects with Tourette Disorder Number:NCT03661983Document
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How to fill out a randomized placebo-controlled trial
How to fill out a randomized placebo-controlled trial
01
Obtain ethical approval from an Institutional Review Board (IRB)
02
Recruit participants who meet the eligibility criteria
03
Randomly allocate participants into either the treatment group or the control group
04
Administer the treatment to the treatment group and a placebo to the control group
05
Collect data on the outcomes of interest
06
Analyze the data to determine the efficacy of the treatment
Who needs a randomized placebo-controlled trial?
01
Researchers conducting clinical trials to test the effectiveness of a new treatment
02
Regulatory agencies evaluating the safety and efficacy of a new drug or intervention
03
Healthcare providers looking to assess the effectiveness of different treatment options
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What is a randomized placebo-controlled trial?
A randomized placebo-controlled trial is a type of study where participants are randomly assigned to either receive the treatment being tested or a placebo, and neither the participants nor the researchers know who is receiving which.
Who is required to file a randomized placebo-controlled trial?
Researchers conducting clinical trials are required to file a randomized placebo-controlled trial.
How to fill out a randomized placebo-controlled trial?
To fill out a randomized placebo-controlled trial, researchers need to design the study, recruit participants, randomize the allocation of treatment, collect data, and analyze the results.
What is the purpose of a randomized placebo-controlled trial?
The purpose of a randomized placebo-controlled trial is to determine the effectiveness of a new treatment and to minimize bias in the results.
What information must be reported on a randomized placebo-controlled trial?
Information such as study design, participant demographics, treatment allocation, outcomes measured, and statistical analysis must be reported on a randomized placebo-controlled trial.
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