Can a simple stitch pattern reduce bleeding in repeat C-Sections?
NCT ID NCT07758959
First seen Aug 11, 2026 · Last updated Aug 12, 2026 · Updated 1 time
Summary
This trial tests two surgical stitching techniques—purse-string versus transverse mattress—to see which controls bleeding better in women with thinned uterine scars undergoing a repeat cesarean section. Participants are randomly assigned to one method, and doctors measure how quickly bleeding stops and how many extra stitches are needed. The goal is to find a safer, more efficient way to manage this common surgical challenge.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Purse-string suture or transverse mattress suture procedure
- What this could lead to
- If one technique proves faster and more effective, it could become the preferred method to reduce bleeding complications in repeat cesarean sections.
- What could go wrong
- This is a small, early-stage trial with only 60 participants, so results may not apply broadly. Surgical outcomes can vary by surgeon skill and patient anatomy.
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
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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
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60 people
The number who actually took part.
- Started
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Aug 2026
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 40 years
- Sex
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Female participants only
- Healthy volunteers
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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 Hide 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: * Females aged 18 to 40 years. * Gestational age \>37 weeks at the time of delivery. * Parity \<5. * History of one or more previous cesarean sections. * Intraoperative evidence of a thinned-out lower uterine segment scar during repeat cesarean section. Exclusion Criteria: * Preeclampsia (blood pressure ≥140/90 mmHg with proteinuria \>+1 on dipstick). * Gestational diabetes mellitus. * Placental abnormalities, including placenta previa, placenta accreta spectrum (accreta/increta), or placental abruption. * Previous uterine repair scar. * Coagulation disorder (prothrombin time \>15 seconds).
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Lahore general hospital
Lahore, Punjab Province, 54070, Pakistan