Randomized clinical trial attesting the effectiveness of perioperative antimicrobial agents according to the result of preoperative bile culture in patients undergoing biliary reconstruction.
Not Applicable
- Conditions
- Hepato-biliary-pancreatic diseases
- Registration Number
- JPRN-UMIN000001278
- Lead Sponsor
- Hokkaido university hospital gastroenterological sutgery II
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with renal dysfunction, sever liver dysfunction or a history of antimicrobial agents -induced allergy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the incidence of SSI occurrence rates within postoperative 30 days between 2 groups (therapeutic usage of antimicrobial agents treated as Class3 by CDC guideline and prophylactic usage of antimicrobial agents recommended by CDC guideline as Class2).
- Secondary Outcome Measures
Name Time Method