- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03602352
A Study of the Cost for Patients Operated for Adhesive Obstruction (SBO) During a Five-year Period
A Cohort Study of the Cost for Patients Operated for Adhesive Obstruction (SBO) During a Five-year Period
Study Overview
Status
Conditions
Detailed Description
It is a population-based cohort study of the costs for patients operated for adhesive small bowel obstruction during a five-year period (2007-2012) in two Swedish neighboring regions. Patients were identified by a broad search of operation and International Classification of Diseases (ICD) codes. Data regarding surgery and complications has been analyzed in a previous study (Clinical trials no NCT0353459)
The costs for hospital stay, radiology, Intensive Care Unit (ICU)-care, operation for the index SBO care event were calculated. The cost for revisit, sick leave and recurrent SBO during follow-up were calculated. Patients were followed to 31st January 2017, last medical note or death.
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Above18 years of age
- Surgery for adhesive surgical bowel obstruction (SBO)
Exclusion Criteria:
• Surgery for SBO of other etiology than adhesions
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cost for primary hospital admission in patients who underwent SBO surgery during 2007-2012
Time Frame: 2007-2012
|
Per 100 000 inhabitants and year
|
2007-2012
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Cost for further hospital admissions, surgery and outpatient visits during follow-up
Time Frame: 2007-2012
|
2007-2012
|
|
Potential cost-reduction with prophylactic treatment calculating with different prophylactic efficacy levels
Time Frame: 2007-2012
|
2007-2012
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Urban Karlbom, MD PhD, Region Uppsala
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ASBO-02
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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