Single Dose Versus Double Dose Tamsulosin 0.4 and Solifenacin 5 in Management of Stent Related Symptoms
NCT06955533 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 64
Last updated 2025-05-02
Summary
This study was a randomized clinical trial conducted on 64 Egyptian patients from the outpatient clinic at Ain Shams University Hospital over a six-month period from 3/2024 to 9/2024.The study population was randomized into 2 groups. Group A included 32 patients with stent related symptoms receiving double doses of tamsulosin (Tamsulin® 0.4 mg 2 capsules taken together per day) and Solifenacin 10mg (Sofenacin® 10mg tab taken once daily).Group B included 32 patients with stent related symptoms receiving a standard dose of tamsulosin (0.4 mg once daily) and solifenacin (5 mg once daily).
Conditions
- Stent Related Symptoms
Interventions
- DRUG
-
Double dose tamsulosin and solifenacin
Odd number
- DRUG
-
Single dose tamsulosin and solifenacin
Even number
Sponsors & Collaborators
-
Ain Shams University
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2024-04-01
- Primary Completion
- 2024-08-01
- Completion
- 2024-08-01
Countries
- Egypt
Study Locations
More Related Trials
-
Study of Solifenacin Succinate and Tamsulosin Hydrochloride OCAS in Males With Lower Urinary Tract Symptoms
NCT01018511 ·Status: COMPLETED ·Phase: PHASE3
-
Use of Hyoscyamine Versus Tamsulosin for Management of Ureteral Stent Irritation
NCT03750656 ·Status: TERMINATED ·Phase: PHASE4
-
Efficacy of Mirabegron Versus Tamsulosin Versus Solifenacin for Treatment of Ureteral Stents-Related Symptoms
NCT04325880 ·Status: UNKNOWN ·Phase: PHASE3
-
Clinical Trial to Investigate the Pharmacokinetic Drug Interaction Between Solifenacin and Tamsulosin
NCT02180997 ·Status: COMPLETED ·Phase: PHASE1
-
Efficacy And Safety Study Of Naftopidil to Patients Treatment With LUTS
NCT01203371 ·Status: WITHDRAWN ·Phase: PHASE3
-
Study to Evaluate the Clinical Efficacy and Safety of Tamsulosin Alone or in Combination With Solifenacin for the Treatment in Men With Lower Urinary Tract Symptoms Including Overactive Bladder Symptoms
NCT02715024 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Safety of SL77.0499-10 (Alfuzosin) Versus Placebo and Tamsulosin in Japanese Patients With Benign Prostatic Hyperplasia
NCT00399464 ·Status: COMPLETED ·Phase: PHASE3
-
A Study With Combination Treatment (Tamsulosin Hydrochloride and Solifenacin Succinate) in Male Patients With LUTS/BPH
NCT00510406 ·Status: COMPLETED ·Phase: PHASE2
-
Comparison Between Tamsulosin and Tadalafil in Management of Benign Prostatic Hyperplasia Long Term Study
NCT05818670 ·Status: COMPLETED ·Phase: PHASE4
-
Actual Use Study of Tamsulosin in Men
NCT02573311 ·Status: COMPLETED ·Phase: PHASE3
-
Solifenacin as Add-on Therapy for Overactive Bladder Symptoms in Men Treated for Benign Prostatic Hyperplasia
NCT00771394 ·Status: COMPLETED ·Phase: PHASE4
-
(Phosphodiesterase 5 Inhibitors & α-blockers): Single Versus Combined Therapy in Benign Prostatic Hyperplasia
NCT05236634 ·Status: UNKNOWN ·Phase: NA
-
Medications for Lower Urinary Tract Symptoms Secondary to Benign Prostatic Hyperplasia
NCT06491108 ·Status: RECRUITING ·Phase: PHASE3
-
The Efficacy and Safety of Silodosin Singly or Combined With Ningmitai Capsules in the Treatment of Benign Prostatic Hyperplasia
NCT05551221 ·Status: RECRUITING ·Phase: PHASE4
-
Administration of Tadalafil in Patients With Benign Prostatic Hyperplasia
NCT06466369 ·Status: COMPLETED ·Phase: PHASE3
-
Dutasteride and Flex Dose of Tamsulosin on as Needed Basis, to Treat Benign Prostatic Hyperplasia
NCT00701779 ·Status: COMPLETED ·Phase: PHASE4
-
The PK Study of the JLP-1207 and Solifenacin/Tamsulosin in Healthy Male Volunteers.
NCT02494349 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of Tadalafil in Men With Benign Prostatic Hyperplasia
NCT00970632 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate How Tamsulosin (at 1 Dose) and Solifenacin (at 2 Different Doses) Are Taken up From the Intestine, Distributed Through the Body and Eliminated From the Body When Administered in Combination as a Single Tablet (Called EC905)
NCT01953848 ·Status: COMPLETED ·Phase: PHASE1
-
The Effects of α-adrenergic Receptor Antagonists on Choroid and Pupil
NCT03144596 ·Status: COMPLETED ·Phase: PHASE4
-
A Study To Compare 3 Different Formulations Of Tamsulosin At Steady State.
NCT00609596 ·Status: COMPLETED ·Phase: PHASE1
-
Long Term Study of Solifenacin Succinate and Tamsulosin Hydrochloride Oral Controlled Absorption System (OCAS) in Males With Lower Urinary Tract Symptoms
NCT01021332 ·Status: COMPLETED ·Phase: PHASE3
-
Observational Study of Tamsulosin in Patients With Benign Prostatic Hyperplasia
NCT02245555 ·Status: COMPLETED
-
EC905 Pharmacokinetic Profile Study
NCT02634489 ·Status: COMPLETED ·Phase: PHASE1
-
Clinical Trial to Compare the Solifenacin/Tamsulosin Combination Therapy With Tamsulosin Monotherapy for LUTS Due to BPH
NCT02972268 ·Status: COMPLETED ·Phase: PHASE3