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Comparative Study on the Clinical Efficacy of Mirabegron and Doxazosin in Alleviating Ureteral Stent Symptoms

Comparative Study on the Clinical Efficacy of Mirabegron and Doxazosin in Alleviating Ureteral Stent Symptoms

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095161
Enrollment
Unknown
Registered
2025-01-02
Start date
2023-01-09
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Ureteral Stent-Related Dysfunction

Interventions

mirabegron :Patients were randomly divided into two groups, this group of patients treated with mirabegron (50 mg/day).
doxazosin:Patients were randomly divided into two groups, this group of patients treated with doxazosin (4 mg/day)

Sponsors

Kunming Health Commission
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adult male or female patients > 18 years of age with urinary calculi confirmed by imaging (CT or ultrasound) and requiring transurethral ureteral lithotripsy and ureteral stent implantation.

Exclusion criteria

Exclusion criteria: 1. History of overactive bladder, interstitial cystitis, pelvic pain, or pelvic surgery; 2. Patients with severe gynecological diseases, malignant tumors, heart and lung failure, or severe infection and shock symptoms; 3. Patients with psychiatric disorders; 4. BMI >=40 kg/m²; 5. Long-term use of contraceptive pills, digoxin, nebivolol, propranolol, and nadolol (known to interfere with ß3AR signaling); 6. Patients continuously receiving sildenafil or other PDE5 inhibitors; 7. Participants in any other interventional trials; 8. Patients unable to provide informed consent (those under legal guardianship); 9. Drug contraindications (such as hypersensitivity reactions).

Design outcomes

Primary

MeasureTime frame
Ureteral stent symptom;

Countries

China

Contacts

Public ContactBo Tao

The Affiliated Anning First People's Hospital, Kunming University of Science and Technology,

tb13529151395@163.com+86 135 2915 1395

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026