Optimization of methods for assessing level III defects in pelvic organ prolapse

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400089832

Enrollment

Unknown

Registered

2024-09-18

Start date

2024-09-18

Completion date

Unknown

Last updated

2024-09-23

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

Conditions

pelvic organ prolapse

Interventions

Experiment group:III level repair

Control group:No III level repair

Eligibility

Sex/Gender

Female

Age

30 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Fulfillment of the clinical diagnostic criteria for POP (anterior, middle and posterior pelvic prolapse); (2) Performed POP surgery; (3) All patients voluntarily enrolled in this study and signed an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Severe medical comorbidities; (2) Coagulation disorders; (3) Acute exacerbation of inflammation; (4) Vaginal ulcers;

Design outcomes

Primary

Measure	Time frame
POP-Q staging;	—

Secondary

Measure	Time frame
PFDI-20;PISQ-12;	—

Countries

China

Contacts

Public ContactXin Yang

Peking University People's Hospital

xinyang_2003@sina.com+86 10 8832 4350

Outcome results

None listed

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