Clinical Trials Directory

Trials / Completed

CompletedNCT02244333

Efficacy, Tolerability and Safety of ALNA® in Patients With Benign Prostatic Syndrome (BPS)

ALNA® - AWB in Pre-treated Patients With BPS

Status
Completed
Phase
Study type
Observational
Enrollment
4,575 (actual)
Sponsor
Boehringer Ingelheim · Industry
Sex
Male
Age
Healthy volunteers
Not accepted

Summary

Study to assess efficacy, tolerability and safety parameters of a one month ALNA® - treatment after switch from Terazosin-treatment

Conditions

Interventions

TypeNameDescription
DRUGALNA®

Timeline

Start date
2004-02-01
Primary completion
2004-07-01
First posted
2014-09-19
Last updated
2014-09-19

Source: ClinicalTrials.gov record NCT02244333. Inclusion in this directory is not an endorsement.