Ethical issues arising when interim data in clinical trials is restricted to independent data monitoring committees

IRB. 2000 Jan;22(1):7-11.

Authors

R J Wells¹, P S Gartside, C L McHenry

Affiliation

¹ College of Medicine, University of Cincinnati, OH, USA.

PMID: 12546010

No abstract available

MeSH terms

Access to Information / ethics*
Clinical Trials Data Monitoring Committees / ethics*
Clinical Trials Data Monitoring Committees / standards*
Humans
Informed Consent
Probability
Randomized Controlled Trials as Topic / ethics*
Research Design
Research Personnel
Research Subjects
Uncertainty