Clinical Trials Directory

Trials / Completed

CompletedNCT07312955

Solifenacin Plus Tadalafil vs Solifenacin Alone for Overactive Bladder in Females

Efficacy of Combination of Solifenacin and Tadalafil Versus Solifenacin Alone in Treatment of Overactive Bladder in Females

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Ain Shams University · Academic / Other
Sex
Female
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Overactive bladder (OAB) is characterized by urinary urgency with or without urge urinary incontinence, usually with frequency and nocturia, in the absence of urinary tract infection or other obvious pathology. Antimuscarinic agents such as solifenacin are commonly used but may provide incomplete symptom control. Tadalafil (a Phosphodiesterase type 5 inhibitorsinhibitor) has been reported to improve lower urinary tract symptoms and may offer additional benefit in overactive bladder. This randomized controlled trial evaluates the efficacy and tolerability of solifenacin 5 mg plus tadalafil 5 mg versus solifenacin 5 mg alone in females with overactive bladder using the Overactive Bladder Symptom Score (OABSS).

Conditions

Interventions

TypeNameDescription
DRUGSolifenacinSolifenacin 5 mg oral tablet, once daily for 3 months.
DRUGTadalafilTadalafil 5 mg oral tablet, once daily for 3 months.

Timeline

Start date
2025-05-15
Primary completion
2025-11-15
Completion
2025-11-15
First posted
2025-12-31
Last updated
2025-12-31

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT07312955. Inclusion in this directory is not an endorsement.