Randomized controlled trial to evaluate the effects of the surgical instrument LigaSure on reduction of time of liver transection time, compared with the conventional clamp crushing method at the single institutio
Phase 3
- Conditions
- Patients undergoing liver resection.
- Registration Number
- JPRN-C000000337
- Lead Sponsor
- Hepato-Biliary-Pancreatic Surgery Division, Department of Surgery, Tokyo University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Not provided
Exclusion Criteria
1.Simultaneous development of other malignant disease (except a colorectal carcinoma associated with liver metastasis) 2.Cases with high-risks of bleeding, for example; platele counts < 50000/mm3, bleeding time > 5min., PT% < 50% 3.Cases in which inflow occulusion is impossible. 4.Cases with bilio-enteric reconstruction 5.Emergency operation case 6.Cases with some complications of heart, lung, and kidney.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method iver transection time in hepatectomy
- Secondary Outcome Measures
Name Time Method Transection area per minute, total operation time, total amount of bleeding, amount of bleeding during transection, amount of transfusion, incidence of bile leakage, postoperative bleeding, incidence of pleural effusion/ascites, hospital stay, postoperative iver function, total bilirubin value of the drained discharge