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Patients & Volunteers

Understanding Clinical Trials

New medicines are being discovered and developed all around the world all the time. These new medicines are tested in laboratories and in animal studies to ensure that they work and are safe for human use. Medicines that pass these tests are then allowed to be given to a limited number of healthy human volunteers and patients in a controlled manner before they can be released for general use. Early human use of an experimental medicine is called a ‘Clinical Trial’. These help to confirm the effectiveness and safe use of the new medicines. The government requires these trials to be conducted before a new medicine can be approved for general use.

Understanding Clinical Trials
Clinical Trials at Medanta

Clinical Trials at Medanta

There are several clinical trials ongoing at Medanta at any time. Healthy volunteers and patients eligible for these trials are asked whether they would like to participate. Patients interested in participating in a trial are explained the benefits, and risks of participation. Only patients who agree to participate after reading an informed consent document and signing a consent form are included in a clinical trial.

Risks and Benefits of Participating in Clinical Trials

Risks and Benefits of Participating in Clinical Trials

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Clinical Trials and Eligibility

Clinical Trials and Eligibility

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