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New stitch technique may reduce uterine scar defects after C-Section

NCT ID NCT07229222

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

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 a new way of stitching the uterus after a first-time C-section to see if it could prevent a scar defect called a 'niche.' 380 women were randomly assigned to get either the new stitch method or the standard one. The researchers then used ultrasound to check for niches 6 months later. The goal was to find a better surgical technique to improve long-term uterine healing.

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

380 people

The number who actually took part.

Started

Feb 2025

Finished

Dec 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

18 to 45 years

Sex

Female participants only

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: * Acceptance to participate and willingness to attend follow-up for 6 months postpartum. * No plans for pregnancy within the follow-up period. Exclusion Criteria: * Known Müllerian anomalies or uterine fibroids. * Previous uterine surgery. * Multiple gestation. * Chorioamnionitis, placenta previa, or placental abruption. * Preeclampsia/eclampsia. * Hepatic or renal dysfunction, uncontrolled diabetes, or systemic disease. * Peripartum hemoglobin \< 10 g/dL. * Chronic corticosteroid use or smoking. * Inability to provide consent.

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As listed by the trial registrant

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

Cesarean section complications Myometrial remodeling Scar niche Suture techniques

Contacts and locations

Locations

  • Benha Univesity Hospital

    Banhā, Qalyubia Governorate, 13512, Egypt

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