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Not yet recruiting NCT06799208

Laparoscopic Approach in Adhesive Intestinal Obstruction

Observational Efficacy of Laparoscopic Adhesiolysis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Laparoscopy.
Who it may be relevant to
Registry conditions: Efficacy of Laparoscopic Adhesiolysis. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Evaluating the Efficacy of Laparoscopic Approach in Adhesive Intestinal Obstruction

Overview

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

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 .

Interventions

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

Primary outcome measures

  • Number of days post- operative till passing stool . [Time frame: 1 year]

Eligibility criteria

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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06799208 · Laparoscopic adhesiolysis

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗