a multi-center, phaseII, prospective randomized study to investigate optimal duration of prophylactic antimicrobial agent in patients who undergo pancreatico-duodenectomy following preoperative biliary drainage
Not Applicable
- Conditions
- Patients without a symptom of cholangitis who have a planned pancreaticoduodenectomy following preoperative biliary drainage.
- Registration Number
- JPRN-UMIN000007277
- Lead Sponsor
- Department of Surgery, Kansai Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Not provided
Exclusion Criteria
1. a patient with a symptom of cholangitis after preoperative biliary drainage. 2. a patient with anaerobic bacteria detected after preoperative biliary drainage. 3. a patient with resistant bacteria detected after preoperative biliary drainage. 4. a young patient and a patient who has difficulty in self-decision-making 5. a patient who is inappropriate for study entry by a chief doctor
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Frequency of surgical site infection
- Secondary Outcome Measures
Name Time Method