A clinical study for evaluating the utility and safety of robot-assisted gynecologic surgery using da Vinci Si surgical system
Phase 1
Recruiting
- Conditions
- cervical cancer, endometrial cancer, atypical endometrial hyperplasia, uterine myoma
- Registration Number
- JPRN-UMIN000014660
- Lead Sponsor
- niversity of Tsukuba Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who are not recommended for laparoscopic surgery or study enrollment because of complications and other factors
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Anesthesia time, operative time, blood loss, intraoperative and postoperative complications, postoperative pain and hospital stay
- Secondary Outcome Measures
Name Time Method umber of removed lymph nodes, postoperative levels of hemoglobin (Hb), white blood cells (WBC) and C-ractive proteins (CRP), and fever