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A clinical trial to evaluate the safety and efficacy of laparoscopic-assisted endometrial cancer staging (total hysterectomy with double adnexectomy and pelvic lymph node resection)

A clinical trial to evaluate the safety and efficacy of laparoscopic-assisted endometrial cancer staging (total hysterectomy with double adnexectomy and pelvic lymph node resection)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082914
Enrollment
Unknown
Registered
2024-04-10
Start date
2024-04-10
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Staging of endometrial cancer (total hysterectomy and pelvic lymph node dissection)

Interventions

Sponsors

Peking Union Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Diagnosis of intrauterine membrane carcinoma, and preoperative diagnosis of stage I (FIGO 2009 stage) by imaging examination; (2) Endometrial carcinoma was diagnosed by curettage; (3) Aged 18-80 (inclusive); (4) Be able to cooperate and complete follow-up and related examinations; (5) Voluntarily participate in this trial and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) have a severe uncontrolled illness or acute infection; Patients with cardiovascular, cerebrovascular, immune system and diabetes mellitus who can not be controlled and can not meet the operation criteria; (3) Diagnostic curettage revealed serous carcinoma, clear cell carcinoma and carcinosarcoma; (4) Preoperative adjuvant therapy such as radiotherapy and chemotherapy; Radiographically positive pelvic or para-aortic lymph nodes;(6) Poor vaginal conditions, unable to complete uterine extraction (as assessed by the investigator); (7) There are severe pelvic and abdominal adhesions, which are not suitable for laparoscopic surgery; (Viii) participating in other clinical trials of investigational drugs or devices that have not been completed.

Design outcomes

Primary

MeasureTime frame
Rate of unconverted surgery;

Secondary

MeasureTime frame
Operation time;Intraoperative bleeding;Intraoperative blood transfusion;

Countries

china

Contacts

Public ContactXiang Yang

Peking Union Hospital, Chinese Academy of Medical Sciences

Xiangy@pumch.cn+86 135 1105 0222

Outcome results

None listed

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