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Mesh may cut hernia risk after stoma reversal, small trial suggests

NCT ID NCT06157645

Disease control Sponsor: Assiut University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether placing a mesh (a supportive screen) during stoma reversal surgery could prevent hernias better than standard closure. 62 patients who had a temporary stoma took part. The researchers measured hernia rates, infections, pain, and hospital stay length.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Prolene mesh
What this could lead to
If successful, using a mesh during stoma closure could lower the chance of developing a hernia at the surgical site.
What could go wrong
This is a small, single-center trial with only 62 participants. Results may not apply to everyone, and mesh could increase infection risk.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

62 people

The number who actually took part.

Started

Sep 2024

Finished

Sep 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

16 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Patients who are fit for aesthesia. * Patients with temporary double barrelled and simple loop ostomy * Patients older than 16 years old Exclusion criteria: * Patients with end ostomy * Infected stomas

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Conditions

The condition(s) this trial relates to.

Incisional Hernia Pain, Postoperative Surgical Wound Infection

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Complication Hospital stay, length of stay in hospital from surgery to discharge Incisional hernia Postoperative pain Surgical site infection

Contacts and locations

Locations

  • Assiut university hospitals

    Asyut, Asyut Governorate, Egypt

More trials for these conditions

Other studies related to the condition(s) this trial covers.