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OFFICIAL TITLE: A Phase 2,Randomized, Double blind, PlaceboControlled Efficacy, Pharmacokinetics and Safety Study of CA008 in Subjects Undergoing Total Knee Arthroplasty NCT NUMBER: NCT03731364DOCUMENT
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How to fill out a double-blinded placebo-controlled randomized

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How to fill out a double-blinded placebo-controlled randomized

01
Obtain approval from an ethics committee or review board for the study design and protocol.
02
Identify and recruit participants meeting the criteria for the study.
03
Randomly assign participants to either the treatment or control group.
04
Prepare identical looking placebos to be used in the control group.
05
Administer the treatment and placebos to the respective groups while keeping the identity of the treatment blinded to both the participants and researchers.
06
Collect and analyze the data without knowing which participants received the treatment or the placebo.
07
Unblind the study once the data analysis is complete to determine the efficacy of the treatment.

Who needs a double-blinded placebo-controlled randomized?

01
Researchers conducting clinical trials to evaluate the effectiveness of a new medication or treatment.
02
Regulatory agencies requiring robust evidence of a treatment's efficacy before approval for public use.
03
Patients looking for reliable and unbiased results from medical studies to make informed decisions about their health.
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A double-blinded placebo-controlled randomized is a type of clinical trial where both the participants and the researchers are unaware of who is receiving the treatment and who is receiving the placebo.
Researchers conducting clinical trials are required to file a double-blinded placebo-controlled randomized.
To fill out a double-blinded placebo-controlled randomized, researchers must carefully follow the protocol set out in the study design.
The purpose of a double-blinded placebo-controlled randomized is to reduce bias and accurately assess the effectiveness of a new treatment.
Researchers must report detailed information on the study design, participants, interventions, outcomes, and statistical analyses.
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