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CompletedNCT07716709Updated Jul 21, 2026

Bowel Obstruction Post Open Versus Laparoscopic Appendectomy

An interventional study of Open appendectomy and Laparoscopic appendectomy in Bowel Obstruction, sponsored by Sohag University. Completed at 1 site in Egypt. Open to participants aged 12 Years and older. Per ClinicalTrials.gov, last updated 2026-07-21.

Sponsored by Sohag University · Not applicable, Interventional, and Diagnostic

From the registry’s dates

  • Registered 11 months after the study started (first participant enrolled Jul 2025, registered Jun 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
12 Years and older
Sex
All
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Study summary

Acute appendicitis is one of the most common causes of acute abdominal pain requiring surgical intervention, with appendectomy being the definitive treatment . Traditionally performed through an open approach, appendectomy has evolved significantly with the advent of minimally invasive surgery. Since its introduction in the late 1980s, laparoscopic appendectomy has gained widespread acceptance and is now often preferred due to its well-documented advantages, including reduced postoperative pain, shorter hospital stay, quicker return to normal activity, and improved cosmetic outcomes . Despite these benefits, concerns remain regarding the long-term postoperative complications associated with both laparoscopic and open approaches, one of the most clinically significant being bowel obstruction

Read the detailed description

Postoperative bowel obstruction, often resulting from intra-abdominal adhesions, is a common and sometimes serious complication following abdominal surgeries. The pathogenesis of these adhesions can be influenced by several factors, including the extent of tissue handling, exposure of peritoneal surfaces, the degree of inflammation presents during surgery, and the surgical technique used .

Open surgery, by its nature, involves a larger incision and greater manipulation of intra-abdominal structures, which may predispose patients to more extensive adhesion formation and, subsequently, higher rates of bowel obstruction. On the other hand, laparoscopic surgery, with its minimal access approach, is associated with less tissue trauma and reduced adhesion formation in various abdominal procedures. However, it is not entirely devoid of risk, and rare but serious complications such as internal herniation and port site adhesions can also lead to bowel obstruction in laparoscopic cases .

The clinical presentation of postoperative bowel obstruction can vary widely, ranging from mild intermittent symptoms to complete mechanical obstruction requiring urgent reoperation. Understanding the relative risk and nature of bowel obstruction following laparoscopic versus open appendectomy is essential for both surgical decision-making and informed patient counseling. Moreover, identifying differences in the timing, severity, and management outcomes of this complication between the two surgical approaches may help refine perioperative strategies to minimize patient morbidity .

While several studies have attempted to compare postoperative outcomes between laparoscopic and open appendectomy, data specifically focusing on the incidence and characteristics of bowel obstruction are less abundant and sometimes conflicting . Some retrospective reviews suggest a lower incidence of bowel obstruction following laparoscopic appendectomy, while others report no significant difference. Variations in surgical technique, patient selection, underlying pathology, and follow-up duration may all contribute to these discrepancies .

02

Conditions studied

  • Bowel Obstruction

Keywords

  • post appendectomy bowel obstruction
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In context

Intestinal Obstruction

104 studies on the registry are indexed under Intestinal Obstruction; 15 are open to participants now.

This study's enrollment of 50 is below the median of 62 across 54 interventional studies indexed under Intestinal Obstruction.

Browse Intestinal Obstruction studies →

Lead sponsor

Sohag University is the lead sponsor of 1,230 studies on the registry; 636 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
12 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • both genders
  • confirmed diagnosis of acute appendicitis
  • patients undergo laparoscopic or open appendectomy

Exclusion criteria

Exclusion Criteria:

  • appendectomy performed as apart of another operation
  • prior history of abdominal surgery
  • patients show generalized peritonitis
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
50 participants (actual)

Study arms

  • Active comparator
    Group A

    Procedure: Open appendectomy

  • Active comparator
    Gruop B

    Procedure: Laparoscopic appendectomy

Interventions

  • ProcedureOpen appendectomy

    Open appendectomy For gruop A

  • ProcedureLaparoscopic appendectomy

    Laparoscopic appendectomy for group B

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What researchers measure

Primary outcomes

  1. Incidence of bowel obstruction post laparoscopic versus open appendectomy

    Time frame: 6 months

Secondary outcomes

  1. • Operative time

    Time frame: : During operation (from incision to closure)

  2. Analgesic requirement

    Time frame: From postoperative Day 0 through postoperative Day 7.

  3. Postoperative pain

    Postoperative pain assessed using the Visual Analog Scale (VAS; range 0-10, where 0 indicates no pain and 10 indicates the worst imaginable pain).

    Time frame: Postoperative Day 1.

  4. Post operative hospital stay

    Time frame: From the day of surgery until hospital discharge (average of 2-5 days).

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Study locations

1 site
  • Sohag University Hospitals
    Sohag, Egypt
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References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: Undecided

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07716709
Lead sponsor
Sohag University
Responsible party
Nazeh Philip alabd (resident, Sohag University) — Principal investigator
First posted
Jul 21, 2026
Start date
Jul 1, 2025
Primary completion
May 1, 2026
Completion
Jul 1, 2026
Last update
Jul 21, 2026

Study contacts

osama abdlrahem oraby, professor
study director · Sohag University

Oversight

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

Not currently enrolling

This study is completed, as verified in Sep 2025. You cannot join it, but the record below documents what was studied.

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