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A cohort study on postoperative follow-up of various gynecological operations

A cohort study on postoperative follow-up of various gynecological operations

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200059282
Enrollment
Unknown
Registered
2022-04-28
Start date
2022-05-01
Completion date
Unknown
Last updated
2024-02-26

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

Conditions

Various gynecological methods

Interventions

Various gynecological methods:None

Sponsors

Chengdu Women’s and Children’s Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Patients with benign gynecologic diseases; 2.Aged from 20-55 years old; 3.Have indications for vNOTES or TU-LESS endoscopic oviduct fenestration, salpingectomy, ovarian cystectomy, adnexectomy, hysterectomy, and myomectomy.

Exclusion criteria

Exclusion criteria: 1.Patients with virginity; 2.Suspected pelvic inflammation; 3.Colpostegnosis; 4.Severe pelvic peritoneal adhesion; 5.With history of herniation; 6.For myomectomy, multiple uterine myoma both in the anterior and posterior wall, myoma in the cervix, myoma in broad ligament, and myoma in side uterine wall will be excluded.

Design outcomes

Primary

MeasureTime frame
Sexual function, postoperative pain, etc;

Countries

China

Contacts

Public ContactFeng Dan

Chengdu Women’s and Children’s Central Hospital

xinlicwcch@163.com+86 18716370526

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 15, 2026