Zeitschrift für Evidenz, Fortbildung und Qualität im Gesundheitswesen

Jahrgang 106, Heft 5, 00-2012

Seiten 315-319 (5)

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Moritz N. Wente

Summary

Clinical trials with medical devices need to be considered in terms of the complexity of surgical procedures. Creating the proper environment for the conduct of trials includes improved academic career opportunities in the field of clinical research, methodological competence, and established structures. The challenges and pitfalls in the design of clinical trials involving medical devices are based on aspects such as blinding, placebo, learning curves and surgeons’ expertise. Surgical procedures should be standardised, and a study hypothesis needs to be established which is answerable by a relevant and feasible sample size. Besides the above-mentioned challenges, efficient interactions between authorities, universities, hospitals, and medical device manufacturers are mandatory to allow for quality and relevance of clinical studies in this field.

(As supplied by publisher)

Keywords

klinische Studien; Medizinprodukte; Verblindung; Lernkurve; Placebo; clinical trials; medical devices; blinding; learning curve; placebo

DOI (Digital Object Identifier):   10.1016/j.zefq.2012.05.002