Prospective study of efficacy of negative pressure wound therapy for surgical site infection after hepatobiliary and pancreatic surgery
Not Applicable
Recruiting
- Conditions
- Surgical site infection
- Registration Number
- JPRN-UMIN000018054
- Lead Sponsor
- Multicenter Clinical Study Group of Osaka
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Not provided
Exclusion Criteria
1, Naked blood vessel suspected of bleeding or surgical site infection to directly contact to other organs or the presence of fistula to abdominal cavity. 2, The presence of organ/space surgical site infection 3, As determined by the principal investigator or the sub-investigator the subject is not adequate to participate in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The duration from incidence of surgical site infection to wound healing
- Secondary Outcome Measures
Name Time Method The postoperative hospital stay, the cost of hospitalization, the presence of reopened wound, the presence and degree of adverse events