Prescription Event Monitoring in Patients With Benign Prostatic Hyperplasia (BPH)

NCT02244346 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 811

Last updated 2014-09-19

No results posted yet for this study

Summary

Study to evaluate the safety profile of Secotex® in the improvement of the symptoms of Benign Prostatic Hyperplasia in real clinical practice

Conditions

  • Prostatic Hyperplasia

Interventions

DRUG

Secotex®

Sponsors & Collaborators

Eligibility

Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-05-31
Primary Completion
2004-11-30

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02244346 on ClinicalTrials.gov