- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03663023
Band Adhesions in Relation to Previous Abdominal Surgery
February 22, 2023 updated by: Göteborg University
Band Adhesions in Relation to Previous Abdominal Surgery - a Retrospective Analysis of Risk Factors
This study investigates the prevalence of previous abdominal surgery in a cohort of patients operated for bowel obstruction and analyzes the causes of obstruction discovered at surgery.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Postoperative intra-abdominal adhesions are a common cause of small bowel obstruction.
The extent of adhesions has been assigned to the magnitude of previous surgery.
In a county hospital, with a catchment population of 120 000 inhabitants, records of operations performed for bowel obstruction over a period of 70 months were retrieved.
Codes for bowel obstruction according to an International Classification of Diseases (ICD-10) will include: Intestinal adhesion with obstruction, Other and unspecified intestinal obstruction, Intestinal obstruction and Peritoneal adhesions.
Amount of adhesions will be calculated in relation to previous surgery.
Study Type
Observational
Enrollment (Actual)
196
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
According to the protocol, 213 surgical procedures were identified.
17 procedures were excluded due to no bowel obstruction at surgery.
Intestinal obstruction was evident in 196 procedures.
These procedures were included in this study.
Description
Inclusion Criteria:
Subjects operated for bowel obstruction -from January 1st 2006 to October 31st 2011
Surgical codes for bowel obstruction:
- Intestinal adhesion with obstruction
- Other and unspecified intestinal obstruction
- Intestinal obstruction
- Unspecified and Peritoneal adhesions
Surgical procedures identified for bowel obstruction:
- Division of band adhesion
- Adhesiolysis
- Other separation of adhesion during bowel obstruction
- Laparotomy and reposition or detorsion of intestine.
Exclusion Criterias:
-Extra-peritoneal surgery such as inguinal or ventral hernia repair was excluded.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
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 |
---|---|---|
Cause of bowel obstruction
Time Frame: 70 months
|
Bowel obstruction; caused by adhesions, malignant disease, inflammation or other causes
|
70 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2006
Primary Completion (Actual)
October 31, 2011
Study Completion (Actual)
October 31, 2011
Study Registration Dates
First Submitted
September 6, 2018
First Submitted That Met QC Criteria
September 6, 2018
First Posted (Actual)
September 10, 2018
Study Record Updates
Last Update Posted (Actual)
February 24, 2023
Last Update Submitted That Met QC Criteria
February 22, 2023
Last Verified
February 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Adhesions2018vgr
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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