Elsevier

The Lancet

Volume 354, Issue 9175, 24 July 1999, Pages 327-330
The Lancet

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Clinical trials, consensus conferences, and clinical practice

https://doi.org/10.1016/S0140-6736(98)11185-6Get rights and content

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Limitations and strengths of randomised clinical trials

Randomised clinical trials are powerful tools to test therapies and, when well designed and carried out, they should certainly influence our decision-making. But not even their strongest proponents suggest they are without limits. These limitations are of two types: specific and fundamental. Some of the specific limitations are obvious. Among these are that different dosages of pharmacological agents are rarely examined, and the full potential for benefit or harm from combinations of therapy is

Limitations of consensus conferences

Increasingly, results of randomised clinical trials drive the decisions of consensus conferences, and increasingly the decisions from consensus conferences drive clinical practice. Tests and therapies not approved by consensus conferences are also increasingly unlikely to be reimbursed, and the recommendations of consensus conferences may begin to be adopted as a legally decisive standard for medical practice.5 But a consensus conference is as much a social as a scientific process. And herein

Recommendations

Clinical trials and consensus conferences are irreplaceable and invaluable instruments. The question is not of abandoning them but of strengthening them. The following are suggestions of how we may do so.

Medical journals already help greatly in interpretation of randomised clinical trials by including editorials to assist in the complex process of interpretation. They also help by, from time to time, reviewing principles of interpretation of evidence and fundamentals of statistics. These

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