Laparoscopic Approach in Adhesive Intestinal Obstruction

January 23, 2025 updated by: Mohammad Sayed Mohammad Ibrahim, Assiut University

Evaluating the Efficacy of Laparoscopic Approach in Adhesive Intestinal Obstruction

A Clinical trail to evaluate the efficacy of Laparoscopic approach in Adhesive Intestinal Obstruction .

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

There was a rapid growth of minimally invasive operations. Through its peritoneal tissue sparing character and minimal blood loss, laparoscopy was soon claimed to reduce adhesion formation and associated complications.

The aim of this prospective clinical trial study is to evaluate the use of laparoscopy in management of clinically diagnosed adhesive intestinal obstruction and the criteria of selection to get the best results .

Study Type

Observational

Enrollment (Estimated)

40

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

  • Name: Mohammad Sayed Mohammad Sayed Mohammad Ibrahim, General Surgery Resident
  • Phone Number: 02+01123368767
  • Email: abdeldayem3151998@gmail.com

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

Sampling Method

Non-Probability Sample

Study Population

All patients admitted to General Surgery department with adhesive intestinal obstruction during the year of study.

Description

Inclusion Criteria:

  • Patient who clinically diagnosed as adhesive intestinal obstruction.
  • Both sexes
  • Adult patients (above 18 years old

Exclusion Criteria:

  • • Patient refused to participate in this study.

    • Patients not fit for laparoscopic surgery.

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Patient diagnosed with intestinal obstruction
Procedure: Laparoscopy
Minimal invasive approach. Have peritoneal tissue sparing character . Minimal blood loss . Reduction of postoperative adhesions.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Number of days post- operative till passing stool .
Time Frame: 1 year
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Assiut University

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 (Estimated)

March 1, 2026

Primary Completion (Estimated)

March 1, 2027

Study Completion (Estimated)

May 1, 2027

Study Registration Dates

First Submitted

January 10, 2025

First Submitted That Met QC Criteria

January 23, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 23, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Laparoscopic adhesiolysis

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

Yes

product manufactured in and exported from the U.S.

Yes

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.

Subscribe