Status:
COMPLETED
Questioning Patients About Adverse Medical Events
Lead Sponsor:
University of California, San Francisco
Conditions:
Benign Prostatic Hyperplasia
Eligibility:
MALE
50+ years
Brief 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.
Detailed Description
214 patients involved in a larger randomized controlled trial of the herb, saw palmetto, for benign prostatic hyperplasia were randomly assigned to 3 different methods of adverse event ascertainment a...
Eligibility Criteria
Inclusion
- Male, age \> 49, American Urological Association Symptom Index \> 8
- Max urine flow rate \> 4 and \< 15
Exclusion
- prior prostate cancer or surgery
- use of medications that affect urination
- severe concomitant illness
Key Trial Info
Start Date :
April 1 2002
Trial Type :
OBSERVATIONAL
End Date :
April 1 2003
Estimated Enrollment :
214 Patients enrolled
Trial Details
Trial ID
NCT00187616
Start Date
April 1 2002
End Date
April 1 2003
Last Update
January 24 2024
Active Locations (1)
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1
San Francisco VA Medical Center
San Francisco, California, United States, 94121