High vs. Low Segmental Hysterotomy: Impact on Uterine Wall Defects Post-Cesarean
Recruiting
N/A
Interventional Study
Placenta Accreta Spectrum
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 168 (estimated)
- Sponsor
- Fundacion Clinica Valle del Lili · Other
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About This Trial
The purpose of this clinical trial is to compare the incidence of defects in the uterine wall at the site of the scar (niche) and surgical complications when using high-segment versus low-segment hysterotomy, with both cross-suturing and non-cross-suturing techniques, in pregnant patients undergoing their first cesarean section.
Researchers will compare four arms:
* Low Segment Hysterotomy + Cro…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Pregnant women aged ≥ 18 years.
* Confirmed pregnancy through clinical history or ultrasound between 36 and 42 weeks of gestation.
* Indication by the attending gynecologist for a first cesarean section, either emergent or elective.
Exclusion Criteria:
* History of myometria…
Contacts