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Clinical study of laparoscopic vaginal suspension for the treatment of pelvic organ prolapse in elderly women

Clinical study of laparoscopic vaginal suspension for the treatment of pelvic organ prolapse in elderly women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059601
Enrollment
Unknown
Registered
2022-05-04
Start date
2022-05-01
Completion date
Unknown
Last updated
2024-03-18

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

Conditions

pelvic organ prolapse

Interventions

Group A:Laparoscopic tension-free vaginal abdominal wall suspension
Group B :Transvaginal hysterectomy with anterior and posterior vaginal repair

Sponsors

Huadong Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients with POP-Q staging II ~ IV will be selected, with relevant surgical indications; 2. With or without anterior and posterior vaginal prolapse or cervical elongation; 3. Female adults aged 60 and above; 4. Informed consent and will sign the informed consent; 5. Patients who can be followed up for 1 year after surgery.

Exclusion criteria

Exclusion criteria: 1. Patients with suspected malignant tumor found in preoperative evaluation; 2. Patients with chronic pelvic pain; 3. Patients with a history of trans-vaginal mesh exposure; 4. Patients with immune diseases by long-term steroid hormone use.

Design outcomes

Primary

MeasureTime frame
POP-Q;the quality of life questionnaire;recurrence;

Secondary

MeasureTime frame
complications;

Countries

China

Contacts

Public ContactHuiling Zhu

Huadong Hospital Affiliated to Fudan University

513weiwei@126.com+86 13370018098

Outcome results

None listed

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