A prospective cohort study focusing on the incisional wound complications following the abdominal surgery, multicenter trial
Not Applicable
- Conditions
- Digestive surgery
- Registration Number
- JPRN-UMIN000004723
- Lead Sponsor
- Division of Surgical Infection
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 4000
Inclusion Criteria
Not provided
Exclusion Criteria
complete lararoscopic surgery (except laparoscopic-assisted surgery) Patients who was diagnosed as not adequate for this trial
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms contribute to incisional wound complications after abdominal surgery in digestive disease patients?
How does the NSIS-1 cohort study compare with standard-of-care wound management protocols in abdominal surgery?
Are there specific biomarkers associated with increased risk of incisional wound complications in digestive surgery?
What are the most effective strategies for managing adverse events related to abdominal surgical incisions in digestive surgery patients?
What are the current trends in combination therapies for preventing surgical site infections in abdominal procedures?