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CLINICAL STUDY PROTOCOLStudy Title:A Blinded, PlaceboControlled Extension to Study TRCA301 to Evaluate the Long term Safety and Durability of Effect of TRC101 in Subjects with Chronic Kidney Disease
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A blinded placebo-controlled extension on www.clinicalconnection.com is typically needed by individuals who are already participating in a clinical trial and have been assigned to the placebo group.
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The purpose of a blinded placebo-controlled extension is to provide participants in the placebo group with the opportunity to receive the active treatment being studied after the initial trial.
03
This extension allows these individuals to continue their involvement in the study while receiving the active medication or treatment.
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What is wwwclinicalconnectioncomclinical-trials-froma blinded placebo-controlled extension?
The blinded placebo-controlled extension is a phase of a clinical trial where neither the participants nor the researchers know who is receiving the treatment and who is receiving the placebo.
Who is required to file wwwclinicalconnectioncomclinical-trials-froma blinded placebo-controlled extension?
The researchers conducting the clinical trial are required to file the blinded placebo-controlled extension.
How to fill out wwwclinicalconnectioncomclinical-trials-froma blinded placebo-controlled extension?
The blinded placebo-controlled extension is typically filled out by the researchers involved in the clinical trial, following specific guidelines and protocols.
What is the purpose of wwwclinicalconnectioncomclinical-trials-froma blinded placebo-controlled extension?
The purpose of the blinded placebo-controlled extension is to evaluate the long-term effectiveness and safety of the treatment being studied.
What information must be reported on wwwclinicalconnectioncomclinical-trials-froma blinded placebo-controlled extension?
The blinded placebo-controlled extension may require reporting of adverse events, treatment efficacy, and patient outcomes.
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