Actively Recruiting
Study of Tamsulosin, Solifenacin and Mirabegron in Alleviating Ureteral Stent-related Symptoms
Led by Bir Hospital · Updated on 2025-09-08
189
Participants Needed
1
Research Sites
69 weeks
Total Duration
On this page
Sponsors
B
Bir Hospital
Lead Sponsor
N
Nepal Health Research Council
Collaborating Sponsor
AI-Summary
What this Trial Is About
A comparative study on the efficacy of Tamsulosin, Solifenacin and Mirabegron in alleviating ureteral stent-related symptoms: a randomized controlled trial.
CONDITIONS
Official Title
Study of Tamsulosin, Solifenacin and Mirabegron in Alleviating Ureteral Stent-related Symptoms
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients aged 19 to 80 years
- Underwent unilateral retrograde rigid ureteroscopy or retrograde intrarenal surgery
- Planned ureteric stent insertion for urinary tract stones
You will not qualify if you...
- Use of alpha-blockers, anticholinergics, corticosteroids, calcium channel blockers, or analgesics
- Undergoing percutaneous nephrolithotomy, open or laparoscopic ureteric surgery
- Neurogenic bladder, overactive bladder syndrome, neurological or psychiatric diseases
- Preoperative febrile urinary tract infection
- Pregnancy or breastfeeding
- Having a single kidney
- Moderate or severe cardiovascular or cerebrovascular disease
- Hepatic dysfunction
- History of pelvic surgery or irradiation
- History of bladder or prostate surgery
- Acute medical conditions affecting pain score (e.g., acute pancreatitis, gastroenteritis, musculoskeletal disorders)
- Allergy to any medication
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
NAMS, Bir Hospital
Kathmandu, Bagmati, Nepal, 44600
Actively Recruiting
Research Team
B
Baikuntha Adhikari, MCh
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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