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1CLINICAL PROTOCOL
STUDY NIDACTO0012
PHASE 2, DoubleClick, PLACEBOCONTROLLED TRIAL MAGAZINE FOR THE TREATMENT OF COCAINE DEPENDENCEPrincipal Investigator:
Subinvestigators:Eugene Somoza, M.D., Ph.D.
R.
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How to fill out a double-blind placebo-controlled trial

How to fill out a double-blind placebo-controlled trial
01
Randomly assign participants to either the treatment group or the control group.
02
Ensure that neither the participants nor the researchers administering the treatment know who is receiving the actual treatment and who is receiving the placebo.
03
Monitor and record the outcomes for each group, without knowing which group received the actual treatment until the study is completed.
04
Analyze the results to determine the effectiveness of the treatment compared to the control group.
Who needs a double-blind placebo-controlled trial?
01
Researchers and scientists conducting clinical trials to test the effectiveness of new medications or treatments.
02
Regulatory bodies and health organizations looking for unbiased evidence on the efficacy of a particular treatment.
03
Patients and consumers who want to know if a treatment is truly effective or if it is just a placebo effect.
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What is a double-blind placebo-controlled trial?
A double-blind placebo-controlled trial is a type of experiment where neither the participants nor the researchers know who is receiving active treatment and who is receiving a placebo.
Who is required to file a double-blind placebo-controlled trial?
Researchers and organizations conducting clinical trials are required to file a double-blind placebo-controlled trial.
How to fill out a double-blind placebo-controlled trial?
To fill out a double-blind placebo-controlled trial, researchers must follow a specific protocol, including randomization, blinding, and placebo control.
What is the purpose of a double-blind placebo-controlled trial?
The purpose of a double-blind placebo-controlled trial is to assess the efficacy and safety of a new treatment or intervention.
What information must be reported on a double-blind placebo-controlled trial?
Information that must be reported on a double-blind placebo-controlled trial includes study design, participant demographics, treatment protocols, outcomes, and adverse events.
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