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
| Type | Name | Description |
|---|---|---|
| DRUG | Solifenacin | Solifenacin 5 mg oral tablet, once daily for 3 months. |
| DRUG | Tadalafil | Tadalafil 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.