Clinical Trials Directory

Trials / Unknown

UnknownNCT02827578

Efficacy and Safety of Tamsulosin/Solifenacin Combination Therapy in Patients With Voiding Symptoms and Moderate to Severe Storage Symptoms Due to Benign Prostate Hyperplasia

Efficacy and Safety of Tamsulosin/Solifenacin Combination Therapy in Patients With Voiding Symptoms and Moderate to Severe Storage Symptoms Due to Benign Prostate Hyperplasia : a Randomized, Double Blinded, Parallel Design, Active Controlled, Multi-center, Phase 3 Clinical Trial

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
588 (estimated)
Sponsor
IlDong Pharmaceutical Co Ltd · Industry
Sex
Male
Age
45 Years
Healthy volunteers
Not accepted

Summary

Efficacy and Safety of Tamsulosin/Solifenacin Combination therapy in Patients with voiding symptoms and moderate to severe storage symptoms due to Benign Prostate Hyperplasia : a randomized, double blinded, parallel design, active controlled, multi-center, phase 3 clinical trial

Conditions

Interventions

TypeNameDescription
DRUGTamsulosinTamsulosin
DRUGSolifenacinSolifenacin
DRUGSolifenacin placeboSolifenacin placebo

Timeline

Start date
2016-01-01
Primary completion
2017-08-01
Completion
2017-12-01
First posted
2016-07-11
Last updated
2016-07-13

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02827578. Inclusion in this directory is not an endorsement.

Efficacy and Safety of Tamsulosin/Solifenacin Combination Therapy in Patients With Voiding Symptoms and Moderate to Seve (NCT02827578) · Clinical Trials Directory