A histological cohort study fo assess the adverse events using Adspray in laparoscopic surgery for early uterine endometrial cancer.
Not Applicable
Recruiting
- Conditions
- terine endometrial cancer
- Registration Number
- JPRN-UMIN000041628
- Lead Sponsor
- Tokyo women's medical university
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 300
Inclusion Criteria
Not provided
Exclusion Criteria
1. Patients scheduled for laparotomy. 2. Patients scheduled for surgery without pelvic lymph node dissection. 3. Patients scheduled for para-aortic lymph node dissection. 4. Patients with pelvic infection or infectious diseases requiring treatment. 5. History of obstructive bowel disease. 6. History of pelvic radiation therapy. 7. Patients who are judged to be inappropriate as subject to this study by the physician.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of postoperative infection within 30 days after surgery
- Secondary Outcome Measures
Name Time Method