KCT0002599Recruiting未知
The effect of Mirabegron for the double-J stent discomfort: Randomized, prospective case-control study.
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Recruiting
- Enrollment
- 100
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional Study
Eligibility Criteria
- Ages
- 20(Year) to o Limit (—)
- Sex
- All
Inclusion Criteria
- •Patients to be undergone double J stent indwelling after flexible or rigid ureteroscopic stone removal.
- •1. =20 years
- •2. Undergoing unilateral retrograde double-J (DJ) stent (6Fr) placement planned for 5-28 days indwelling (only after ureteroscopic procedure, retrograde intrarenal surgery)
Exclusion Criteria
- •1. After percutaneous nephrolithotomy, open or laparoscopic ureterolithotomy
- •2. Presence of ureteral stone
- •3. Renal insufficiency (serum Cr > 1.7)
- •4. Febrile UTI (fever > 38°, evidence of urinary infection)
- •5. Pregnancy or breast feeding
- •6. Solitary kidney
- •7. Hypersensitivity to mirabegron
- •8. Current use of any alpha-blocker, calcium-channel blocker, corticosteroid, Anti-muscarinic agents (within 4 weeks)
- •9. Moderate or severe cardiovascular or cerebrovascular disease
- •10. Hepatic dysfunction (>2 x normal LFT)
- •11. Prior history of pelvic surgery or irradiation
- •12. Prior history of TURBT or prostate surgery
- •13. Significant active medical illness which in the opinion of the investigator would preclude protocol treatment
- •14. Genetic disorder such as Galatose intolerance, Lapp Lactase deficiency, Glucose-Galactose malabsorption
Investigators
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