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Efficacy and safety of low-intensity pulsed ultrasound (LIPUS) in treating patient with urinary incontinence after radical prostatectomy (randomized, double-blind, prospective, multicenter clinical trial)

Efficacy and safety of low-intensity pulsed ultrasound (LIPUS) in treating patient with urinary incontinence after radical prostatectomy (randomized, double-blind, prospective, multicenter clinical trial)

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064836
Enrollment
Unknown
Registered
2022-10-19
Start date
2022-10-11
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Urinary incontinence after radical prostatectomy

Interventions

Experimental group:400 mW/cm^2
Control group:0 mW/cm^2

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Subjects fully understand the benefits and risks of this experiment, are willing to participate and sign informed consent; 2. Subjects with urinary incontinence two weeks after removal of urinary tube after radical prostate cancer surgery; 3. Preoperative urinary control was normal, no stress urinary incontinence and other urinary incontinence.

Exclusion criteria

Exclusion criteria: 1. Patients with immunosuppression, dementia, chronic depression or psychosis, multiple cell sclerosis and Parkinson's disease. 2. Urinary incontinence before surgery. 3. If the patient has undergone colon surgery, hemorrhoidectomy, TURP, or bone surgery in the pelvic region within the last three months. 4. Patients with a history of preoperative pelvic radiotherapy. 5. Serious postoperative complications, such as pelvic infection, abscess and cardiopulmonary insufficiency.

Design outcomes

Primary

MeasureTime frame
Frequency of changing pads (full wet);

Secondary

MeasureTime frame
Urinary Incontinence Questionnaire Short Form (ICI-Q-SF);ICI-Q-LUTSqol;Urinary Incontinence Quality of Life Questionnaire (I-QOL);1h pad test;

Countries

China

Contacts

Public ContactHan Bangmin

Shanghai General Hospital

hanbm@163.com+86 18939757031

Outcome results

None listed

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