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A randomized controlled study on the efficacy and safety of transumbilical laparoscopic single site surgery (TU-LSSS) and traditional porous laparoscopic radical surgery for cervical cancer.

A randomized controlled study on the efficacy and safety of transumbilical laparoscopic single site surgery (TU-LSSS) and traditional porous laparoscopic radical surgery for cervical cancer.

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000037611
Enrollment
Unknown
Registered
2020-08-29
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-11-02

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

Conditions

diseases of obstetrics and gynecology

Interventions

1:Transumbilical laparoscopic single site surgery (tu-lsss) for cervical cancer
2:Traditional laparoscopic radical hysterectomy for cervical cancer

Sponsors

Chengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Aged >= 18 years; (2) Patients with early cervical cancer (I a2 - I B1 / II A1) were scheduled to undergo laparoscopic surgery; (3) The vital signs were stable and could tolerate laparoscopic surgery; (4) Patients were able to understand the protocol and willing to participate in the study, and provided written informed consent.

Exclusion criteria

Exclusion criteria: (1) In acute infection stage, deep venous thrombosis or hypercoagulable state, fasting blood glucose > 11.1mmol/l, blood pressure > 160 / 100mmhg, liver and kidney dysfunction, mental disease and other surgical contraindications; (2) Pelvic surgery history, suspected serious pelvic adhesion; (3) Incomplete fertility; (4) Pregnancy.

Design outcomes

Primary

MeasureTime frame
Perioperative complications;

Secondary

MeasureTime frame
average length of stay;Patient Satisfaction;Use rate of analgesics;Results of nuclear magnetic resonance examination half a year after operation;Body Image Scale/Cosmetic Scale;Results of tumor markers half a year after operation;

Countries

China

Contacts

Public ContactLi He

Chengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China

linyh.2007@aliyun.com+86 13881782966

Outcome results

None listed

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