In clinical trials, double-blind means that

Question

Quizplus · Accepted Answer

Double-blind refers to the fact that both the clinician and the patient are unaware of whether the patient is receiving the medication or a placebo during a clinical trial. This is done to minimize bias and ensure that any observed effects of the medication are due to the medication itself, rather than expectations or biases of the people involved in the trial. Options A and D are incorrect as they refer to blindness in the patient or their parents, which is not relevant to the double-blind concept. Option B is also incorrect as it is not related to the concept of double-blind in clinical trials.

In Clinical Trials, Double-Blind Means That