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Clinical observation of milabellone in the treatment of bladder overactivity after prostatectomy

Clinical observation of milabellone in the treatment of bladder overactivity after prostatectomy

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000036134
Enrollment
Unknown
Registered
2020-08-21
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-08-31

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

Conditions

Benign Prostate Hyperplasia

Interventions

trial group:Mirabegron
control group:Nil

Sponsors

The First Affiliated Hospital of Xian Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
50 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Subjects over 50 years old who are scheduled to undergo surgery for benign prostatic hyperplasia; 2. Progressive dysuria and BPH confirmed by B-ultrasound; 3. Benign prostatic hyperplasia operation indications: such as repeated urinary retention, hematuria, bladder stones, recurrent infection, symptoms seriously affectthe quality of life, drug treatment is invalid or unwilling to take medicine; 4. Good compliance, the subjects themselves or their family members can complete the app operation; 5. Voluntarily participate and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Serious cardiovascular and cerebrovascular diseases, important organ dysfunction and other contraindications for BPH surgery; 2. Neurogenic bladder and urethra dysfunction, urethral stricture and other concomitant diseases that affect the surgical effect; 3. Subjects suspected of prostate cancer by PSA and imaging examination; 4. Subjects allergic to Mirabella and its ingredients.

Design outcomes

Primary

MeasureTime frame
OABSS;

Secondary

MeasureTime frame
IPSS;QoL;VAS;

Countries

China

Contacts

Public ContactDalin He

The First Affiliated Hospital of Xi'an Jiaotong University

hedl@mail.xjtu.edu.cn+86 13991288221

Outcome results

None listed

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