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Effect of Mirabegron for the ureteral stent

The effect of Mirabegron for the double-J stent discomfort: Randomized, prospective case-control study.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CRIS
Registry ID
KCT0002599
Enrollment
100
Registered
2017-12-15
Start date
2017-08-23
Completion date
Unknown
Last updated
2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : Case : Mirabegron 50mg once a day for 2 weeks Control : No additional treatment for 2weeks

Sponsors

Korea University Ansan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
USSQ urinary symptom score (Body pain score)

Secondary

MeasureTime frame
USSQ general health score;USSQ work performance score;IPSS (International prostate symptom score)/ QoL score;additional analgesics use;Post voiding residual urine volume

Countries

Korea, Republic of

Contacts

Public ContactBum Sik Tae

Korea University Ansan Hospital

bumsik4ever@hanmail.net+82-31-412-5192

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026