The participants in the trial must sign an informed consent form before starting the trial. However the informed intent form also tells them that because this was a triple blind placebo controlled trial, they may or not receive Prurisol; they may receive a placebo instead.
Inclusion Criteria:
Evidence of a personally signed and dated written informed consent to participate in the clinical study
we have already discussed the patients can know what drug they are taking especially if you look at the ads by hri trials who DO have affiliates in San Antonio.....so it is an almost definite possibility that people know the name of the drug....imho