Questioning Patients About Adverse Medical Events
NCT00187616 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 214
Last updated 2024-01-24
Summary
This trial studies whether 3 different methods of asking patients about adverse medical events in a clinical trial affects the rate of reported side effects.
Conditions
- Benign Prostatic Hyperplasia
Sponsors & Collaborators
-
University of California, San Francisco
lead OTHER
Principal Investigators
-
Stephen Bent, MD · University of California, San Francisco
Eligibility
- Min Age
- 50 Years
- Sex
- MALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2002-04-30
- Completion
- 2003-04-30
Countries
- United States
Study Locations
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