- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06446440
Lap Adhesiolysis in Intestinal Obstruction
Comperative Study Between Laparoscopic Adhesiolysis Vs Open Adhesiolysis in Adhesive Intestinal Obstruction
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Adhesive Intestinal obstruction is one of the most common complications after any abdominal surgery.
Adhesions account for 75% of causes of intestinal obstruction. laparoscopic adhesiolysis recently increase in frequency over open adhesiolysis but there is no definit evidence of its superiority. In term of length of hospital stay and morbidity.
adhesive bowel obstruction mainly managed by conservative treatment but some refractory cases needs surgical intervention In this study we will evaluate feasibility and efficacy of using laparoscop in adhesiolysis over open approach .
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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-
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Assiut, Egypt
- Recruiting
- Assiut University hospital
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Contact:
- Assiut university Hospitals
- Phone Number: +2088241-1906
- Email: irbasyut@aun.edu.eg
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- any male or female above 18 years has adhesive Intestinal obstruction
- patient fulfilled the criteria to participate but operated before time of study if adequate data available
- patient in which conservative management is failed
Exclusion Criteria:
- othe casues of intestinal obstruction (other than adhsions)
- shocked patient
- cardiovascular diseases
- coagulopathy
- liver cirrhosis
- intracranial diseases
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Group A
These group will include cases underwent laparoscopic adhesiolysis
|
Laparoscopic adhesiolysis
|
|
Group B
These group will include cases underwent open adhesiolysis
|
Open adhesiolysis
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Recurrence rate
Time Frame: 2 years
|
Signs and symptoms of intestinal obstruction
|
2 years
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- Lap adhesiolysis
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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