NCT07792135

Brief 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.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
9mo left

Started Aug 2026

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress10%
Aug 2026Jun 2027

Study Start

First participant enrolled

August 1, 2026

Completed
17 days until next milestone

First Submitted

Initial submission to the registry

August 18, 2026

Completed
10 days until next milestone

First Posted

Study publicly available on registry

August 28, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2027

Expected
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2027

Last Updated

August 28, 2026

Status Verified

August 1, 2026

Enrollment Period

5 months

First QC Date

August 18, 2026

Last Update Submit

August 25, 2026

Conditions

Keywords

laparoscopic ventral hernia

Outcome Measures

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.

    3 months

Study Arms (1)

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.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-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.

You may qualify if:

  • 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.

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Hernia, Abdominal

Condition Hierarchy (Ancestors)

HerniaPathological Conditions, AnatomicalPathological Conditions, Signs and Symptoms

Central Study Contacts

mohamed montaser ahmed, resident

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Resident Mohamed Montser Ahmed elsayed

Study Record Dates

First Submitted

August 18, 2026

First Posted

August 28, 2026

Study Start

August 1, 2026

Primary Completion (Estimated)

January 1, 2027

Study Completion (Estimated)

June 1, 2027

Last Updated

August 28, 2026

Record last verified: 2026-08