Composite fascial pad sling for male stress urinary incontinence treatment

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400083268

Enrollment

Unknown

Registered

2024-04-19

Start date

2023-05-22

Completion date

Unknown

Last updated

2024-04-22

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

Conditions

Male stress urinary incontinence

Interventions

Experimental group:Composite fascial pad sling

Experimental group:Traditional sling technique

Eligibility

Sex/Gender

Male

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age > 18 years (2) Male patients with SUI who have failed physical conservative treatment (3) Voluntary surgical treatment (4) Subjects have signed an informed consent form

Exclusion criteria

Exclusion criteria: (1) Patients who are unable to tolerate surgery due to their physical condition (2) Unavailability of complete preoperative and postoperative baseline data (3) High rate of missed follow-ups and inability to conduct long-term follow-ups (4) Participation in other clinical studies prior to study entry (5) Patients or their authorized persons are unwilling to sign written informed consent or to comply with the study protocol

Design outcomes

Primary

Measure	Time frame
Urination Diary;Urinal pad test;ICI Urinary Incontinence Questionnaire Short Form (ICIQ-SF);	—

Secondary

Measure	Time frame
International Prostate Symptom Score (IPSS);Quality of life score (QOL);Overactive Bladder Syndrome Symptom Score (OABSS);Urodynamic tests;Cystoscopy and imaging;Residual urine volume;	—

Countries

China

Contacts

Public ContactTao Jin

West China Hospital, Sichuan University

jintao97@scu.edu.cn+86 189 8060 6850

Outcome results

None listed

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