CClinicalTrials.gg
Not yet recruitingNCT06799208Updated Jan 29, 2025

Laparoscopic Approach in Adhesive Intestinal Obstruction

An observational study in Efficacy of Laparoscopic Adhesiolysis, sponsored by Assiut University. Not yet recruiting. Per ClinicalTrials.gov, last updated 2025-01-29.

Sponsored by Assiut University · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
40
Sex
All
01

Study summary

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

Read the 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 .

02

Conditions studied

  • Efficacy of Laparoscopic Adhesiolysis
03

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
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.

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

    • Patient refused to participate in this study.

      • Patients not fit for laparoscopic surgery.
04

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
40 participants (estimated)
Patient registry
No

Groups and cohorts

  • Patient diagnosed with intestinal obstruction

    Procedure: Laparoscopy

Interventions

  • ProcedureLaparoscopy

    Minimal invasive approach. Have peritoneal tissue sparing character . Minimal blood loss . Reduction of postoperative adhesions.

05

What researchers measure

Primary outcomes

  1. Number of days post- operative till passing stool .

    Time frame: 1 year

06

Study locations

No study locations are listed for this record.

07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT06799208
Lead sponsor
Assiut University
Responsible party
Mohammad Sayed Mohammad Ibrahim (DR, Assiut University) — Principal investigator
First posted
Jan 29, 2025
Start date
Mar 2026 (estimated)
Primary completion
Mar 2027 (estimated)
Completion
May 2027 (estimated)
Last update
Jan 29, 2025

Study contacts

Mohammad Sayed Mohammad Sayed Mohammad Ibrahim, General Surgery Resident
Contact
abdeldayem3151998@gmail.com
02+01123368767

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion