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Clinical Trials in TMD Sections
Author Bio
Introduction
The Biopsychosocial Model
Designing Multicenter RCTs
Players in an RCT
Randomization
Trial Design Quality
TMD Case Definition
Endpoints and Outcome Measures
Blinding & Masking
Study Sample Size
Number and Nature of Interventions
Study Length and Follow up
Intent-to-treat Analyses and Sample Size
Compliance
Currently selected section: Multicenter RCTs
Implementing RCTs: Practical Issues
Analysis of TMD Trials
Conclusions
Acknowledgments
Appendix A
Appendix B

 

Chapter 22: Clinical Trials in Temporomandibular: Multicenter RCTs
        

In this section, we identify the more important practical issues that arise when multicenter trials are planned, and offer recommendations that may allow multicenter trials to be undertaken more effectively. It is important to emphasize that these types of trials introduce few new issues or components beyond those that must be considered when undertaking any randomized control trial. The exceptions to this broad statement may be related to:

  • Data management and data analysis;
  • Confidentiality of data; and
  • The inevitable layers of complexity added to data analysis when large trials are conducted in multiple clinical settings.

Rather than introducing considerations that do not arise in single center studies, multicenter trials seem inevitably to intensify virtually every aspect and every stage of the multicenter trial with potential complexities.

The burden of experience and the conventional wisdom in the field seems to reflect that problems encountered when multicenter clinical trials are undertaken almost always flow from errors of omission, principally failure to anticipate the need for communication at every stage and/or failure to communicate with the most relevant or responsible individuals at each stage.

The "bottom line" for a multicenter clinical trial is that all participating centers and all participating investigators must agree to follow common protocols -- not only commonly agreed upon protocols for clinical treatments, but commonly agreed upon and uniformly executed protocols for recruitment, enrollment, randomization, and all aspects of data collection, as well as maintaining confidence in data integrity and protection of the rights of human subjects (Friedman et al., 1998b).

Several of these matters are given more attention in the pages that follow.

 

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