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Not yet recruitingNCT07792135IPOMUpdated Aug 28, 2026

Experience of IPOM Technique in Laparoscopic Ventral Hernia Repair

An observational study in Hernia Abdominal Wall and Laparoscopic, sponsored by Sohag University. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-28.

Sponsored by Sohag University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
30
Ages
18 Years and older
Sex
All
01

Study summary

evaluate the clinical experience of Sohag University Hospital with laparoscopic intraperitoneal onlay mesh repair for ventral hernias, assessing operative feasibility, intraoperative complications, postoperative recovery and short-term surgical outcomes, in order to determine its safety and effectiveness in a regional setting.

Read the detailed description

The present study aims to evaluate the clinical experience of Sohag University Hospital with laparoscopic intraperitoneal onlay mesh repair for ventral hernias, assessing operative feasibility, intraoperative complications, postoperative recovery and short-term surgical outcomes, in order to determine its safety and effectiveness in a regional setting.

02

Conditions studied

  • Hernia Abdominal Wall
  • Laparoscopic

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Keywords

  • laparoscopic ventral hernia
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study will include adult patients with primary ventral hernias who are eligible for elective laparoscopic ventral hernia repair using the IPOM technique

Adult patients aged 18 years or older. Patients diagnosed clinically and/or radiologically with primary ventral hernia.

Patients planned for elective laparoscopic ventral hernia repair using the IPOM technique.

Inclusion criteria

  1. Adult patients aged 18 years or older.
  2. Patients diagnosed clinically and/or radiologically with primary ventral hernia.
  3. Patients planned for elective laparoscopic ventral hernia repair using the IPOM technique.

Exclusion criteria

Exclusion Criteria

  1. Patients unfit for general anesthesia or laparoscopic surgery.
  2. Complicated hernias requiring emergency open surgery, such as strangulated hernia, bowel ischemia, perforation, or generalized peritonitis.
  3. Incisional ventral hernias
  4. Recurrent hernias
  5. Active abdominal wall infection, skin ulceration over the hernia, or contaminated operative field.
  6. Pregnancy.
  7. Refusal to provide informed consent or inability to complete postoperative follow-up.
04

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
30 participants (estimated)
Patient registry
No

Groups and cohorts

  • patients with ventral hernia

    1. Adult patients aged 18 years or older. 2. Patients diagnosed clinically and/or radiologically with primary ventral hernia. 3. Patients planned for elective laparoscopic ventral hernia repair using the IPOM technique.

05

What researchers measure

Primary outcomes

  1. the safety and effectiveness of laparoscopic IPOM repair for ventral hernia,

    The primary outcome will be the safety and effectiveness of laparoscopic IPOM repair for ventral hernia, assessed by postoperative complication rate during the follow-up period.

    Time frame: 3 months

06

Study locations

No study locations are listed for this record.

07

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07792135
Lead sponsor
Sohag University
Responsible party
Mohamed Montaser Ahmed (Resident Mohamed Montser Ahmed elsayed, Sohag University) — Principal investigator
First posted
Aug 28, 2026
Start date
Aug 1, 2026 (estimated)
Primary completion
Jan 1, 2027 (estimated)
Completion
Jun 1, 2027 (estimated)
Last update
Aug 28, 2026

Study contacts

mohamed montaser ahmed, resident
Contact
Mohamed.Montaser@med.sohag.edu.eg
01149140771

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 not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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