Thursday, April 15, 2021 8:48:22 AM
I think your links cleared things up a lot. Thanks.
From https://www.ncbi.nlm.nih.gov/books/NBK546641/
"A double-blind study blinds both the subjects as well as the researchers to the treatment allocation. Triple-blinding involves withholding this information from the patients, researchers, as well as data analysts."
From https://mailchi.mp/ipharminc/innovation-pharma-completes-interim-safety-data-reviewdmc-approves-increased-dosing-frequency-in-phase-2-clinical-trial?e=0e1a610318
"an independent Data Monitoring Committee (DMC) completed its scheduled review of interim safety data in the Company’s randomized, double-blind, placebo-controlled Phase 2 clinical trial"
"Efficacy data was not reviewed by the DMC and remains blinded."
The first link also says this:
"Unblinding may occur during any portion of the blinded clinical trial. Unblinding that occurs before the conclusion of a trial may be a source of bias that the study should document and report. It is the responsibility of all the healthcare professionals involved in a clinical trial, such as physicians, nurses, pharmacists, technicians, and data analysts, to maintain blinding as effectively as possible during the trial and to report any premature unblinding."
It's morally wrong to allow a sucker to keep his money.
......W. C. Fields
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