Condition: Placenta Accreta Spectrum · Sponsor: Fundacion Clinica Valle del Lili
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 + Crossed hysterorrhaphy * High Segment Hysterotomy + Crossed hysterorrhaphy * Low Segment Hysterotomy + Non-Crossed hysterorrhaphy * High Segment Hysterotomy + Non-Crossed hysterorrhaphy Participants will: * Cesarean delivery * Attend a follow up appointment between 6 to 16 weeks post surgery where will be perform a transvaginal sonography.
This description comes directly from the study's public registry record.
Albaro J. Nieto, M.D. · 3319090 · albaro.nieto@fvl.org.co
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| Fundación Valle del Lili | Cali, Valle del Cauca Department, Colombia | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06620432