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A randomized controlled study of transumbilical and transvaginal single port laparoscopic hysterectomy

A randomized controlled study of transumbilical and transvaginal single port laparoscopic hysterectomy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035561
Enrollment
Unknown
Registered
2020-08-13
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Gynecologic diseases

Interventions

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: hysterectomy duto uterine myoma, cervical lesions, endometrial atypical hyperplasia, and acceptance either of the two methods.

Exclusion criteria

Exclusion criteria: 1. Patients with obesity (BMI greater than 30 kg / m2); 2. Those whose uterus volume is larger than 3 months' pregnancy; 3. Patients with history of rectal surgery; 4. Suspected malignant, pelvic inflammatory disease history of patients, genital tract infection; 5. Patients with severe adhesion during operation; 6. Patients with non benign lesions and need frozen pathology; 7. Mental illness affects communication and is difficult to follow up; 8. Patients who are unwilling to sign informed consent.

Design outcomes

Primary

MeasureTime frame
rate of convertion;

Secondary

MeasureTime frame
operation time;blood loss;complication;

Countries

China

Contacts

Public ContactGong Yao

The First Affiliated Hospital of Chongqing Medical University

yao_gong@126.com+86 18623639267

Outcome results

None listed

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