An investigation of the safety and efficacy of robot-assisted laparoscopic surgery for cervical and uterine cancer
Not Applicable
- Conditions
- cervical cancer and uterine cancer
- Registration Number
- JPRN-UMIN000013229
- Lead Sponsor
- Department of Gynecology, Hokkaido University Graduate School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 10
Inclusion Criteria
Not provided
Exclusion Criteria
1. Patient with cervical or uterine cancer with specific subtype of undifferentiated carcinoma, small cell carcinoma, clear cell adenocarcinoma, glassy cell carcinoma. 2. Patients who are judged to be not eligible for the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Operation time, console time, blood loss, intra-operative/post-operative complications will be recorded, which will be compared to those of open surgery for cervical and uterine cancers.
- Secondary Outcome Measures
Name Time Method Histopathological completeness of surgery, number of lymph nodes harvested, post-operative bladder function, 5-year recurrence free survival and the site of recurrence.