Predicting Abdominal Reoperation
Completed
- Conditions
- Abdominal AdhesionSurgery
- Registration Number
- NCT05516420
- Lead Sponsor
- Radboud University Medical Center
- Brief Summary
Nationwide retrospective study, to predict the risk of abdominal reoperation.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 72270
Inclusion Criteria
- All patients undergoing first abdominal or pelvic surgery between June 1st 2009 and June 30th 2011 in Scotland.
Exclusion Criteria
- Positive history for abdominal surgery
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Number of patients with an abdominal reoperation in the study cohort within 5 years postoperatively Number of patients undergoing a reoperation after abdominal surgery
- 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 abdominal adhesion formation after surgery?
How does the risk prediction model from NCT05516420 compare to existing tools for abdominal reoperation forecasting?
Are there specific biomarkers identified in NCT05516420 that correlate with long-term reoperation risk in abdominal and pelvic surgery patients?
What adverse events are commonly associated with abdominal reoperations, and how can they be mitigated based on cohort studies?
What are the current standard-of-care strategies for preventing abdominal adhesions, and how might insights from NCT05516420 improve postoperative outcomes?