Clinical Trials Directory

Trials / Completed

CompletedNCT02244268

Study to Evaluate the Effect of ALNA® (Tamsulosin) on the Primary Symptoms of Benign Prostatic Hyperplasia

Effect of ALNA® (Tamsulosin) on the Primary Symptoms of BPH (Benign Prostatic Hyperplasia) Syndrome

Status
Completed
Phase
Study type
Observational
Enrollment
3,629 (actual)
Sponsor
Boehringer Ingelheim · Industry
Sex
Male
Age
Healthy volunteers
Not accepted

Summary

The aims of this observational study are to identify the primary BPH symptoms responsible for the patients to consult a urologic practice, resulting in the prescription of ALNA®, to assess the clincial efficacy on an improved occupational performance of the patients being still employed. Additionally to obtain relevant information for the 5-year report of experience with this product according to the requirements in § 49, para 6 of the German Medicines Act.

Conditions

Interventions

TypeNameDescription
DRUGALNA®

Timeline

Start date
2000-10-01
Primary completion
2001-12-01
First posted
2014-09-19
Last updated
2014-09-19

Source: ClinicalTrials.gov record NCT02244268. Inclusion in this directory is not an endorsement.