Basic principles of clinical trials - What, how and why?

Citation
K. Unnebrink et M. Pritsch, Basic principles of clinical trials - What, how and why?, MED KLIN, 94(8), 1999, pp. 458-464
Citations number
15
Categorie Soggetti
General & Internal Medicine
Journal title
MEDIZINISCHE KLINIK
ISSN journal
07235003 → ACNP
Volume
94
Issue
8
Year of publication
1999
Pages
458 - 464
Database
ISI
SICI code
0723-5003(19990815)94:8<458:BPOCT->2.0.ZU;2-6
Abstract
Treatment evaluation is one of the most important tasks in medical research . Detailed standards have been developed during the last decades. The efficacy/effectiveness of treatments can only be assessed in comparison to control groups. To guarantee the internal validity of these comparisons , the groups have to be comparable at the beginning of the study. This can be achieved by randomized allocation of patients to treatment. Furthermore, as far as possible patient and physician should be blinded to treatment in order to avoid subjective influences on treatment results. Groups should s till be comparable when analysing the trial, thus an analysis according to the principle of intention-to-treat ("as randomized") should be performed. These indispensable principles for design, conduct and analysis of clinical trials are widely accepted and contribute to reliable and credible results .