Not Yet RecruitingNot Applicable

Short Interpregnancy Interval After One Prior Cesarean Delivery and Risk of Intraoperative Maternal Morbidity

80 participantsStarted 2026-04

Plain-language summary

To determine if a short interpregnancy interval following a prior cesarean delivery is associated with an increased risk of intraoperative maternal morbidity (e.g., hemorrhage, visceral injury, prolonged surgery) during the next cesarean delivery.

Who can participate

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: Pregnant women with history of one previous cesarean delivery Women admmitted for delivery by cesarean delivery during the study period Singleton pregnancy Exclusion Criteria: uterine malformation coagulation abnormalities, hypertension or diabetes before pregnancy, immune-related diseases, and chronic hepatic, renal orcardiac diseases Twin or multiple pregnancies Miscarriage before 28 weeks of gestation; Current placental previa or accrete and risk of PPH patients with medical morbid condition like diabetes, preeclampsia, hypertension, cardiac, renal diseases or patients having obstetrical conditions

What they're measuring

Utrine rupture Bladder injury

Timeframe: 1year

Trial details

NCT IDNCT07525362

SponsorAssiut University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2027-04

Contact for this trial

Hwayda Refaat Sayed, Lecturer

+20 hwayda1997@gmail.com

View on ClinicalTrials.gov More Short Interpregnancy Interval trials