Safety Profile of Secotex ® in Patients With Benign Prostatic Hyperplasia

NCT02245529 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 982

Last updated 2014-09-19

No results posted yet for this study

Summary

The Objective of this study is to conduct a Prescription Event Monitoring (PEM) involving patients treated with Secotex® (Tamsulosin) in "real life" settings. The aim of a PEM is to monitor the safety profile of Secotex® in a cohort of patients with Benign Prostatic Hyperplasia as used in general practice

Conditions

  • Prostatic Hyperplasia

Interventions

DRUG

Tamsulosin

Sponsors & Collaborators

Eligibility

Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-03-31
Primary Completion
2005-09-30

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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 NCT02245529 on ClinicalTrials.gov