Canceled by the investigator. A multicenter observational study of postoperative urinary incontinence after radical prostatectomy

Establishment of intelligent assessment technology and platform for senile urinary incontinence

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200062988

Enrollment

Unknown

Registered

2022-08-26

Start date

2022-09-01

Completion date

Unknown

Last updated

2023-10-09

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

Conditions

Urinary Incontinence

Interventions

Prostatic cancer patient:None

Eligibility

Sex/Gender

Male

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Signed informed consent; 2. Patients who were clinically diagnosed with prostatic cancer and planned to receive radical prostatectomy.

Exclusion criteria

Exclusion criteria: 1. Cognitive dysfunction and poor compliance, unable to use home-based uroflowmetry and leak urine record instruments; 2. Complications of cerebrovascular diseases and nervous system diseases affecting patients' urination (such as Parkinson's disease, myasthenia gravis, spina bifida, etc.); 3. Serious mental and neurological disorders and unable to cooperate with the investigator.

Design outcomes

Primary

Measure	Time frame
Leak volume;Voiding time;Qave;Voided volume;Qmax;Residual urine volume;	—

Countries

China

Contacts

Public ContactYaoguang Zhang

Beijing Hospital

zhang003887@sina.com+86 13031099662

Outcome results

None listed

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