NCT Number: NCT07525362
Short Interpregnancy Interval After One Prior Cesarean Delivery and Risk of Intraoperative Maternal Morbidity
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.
Trial opening soon.
Get NotifiedKey information
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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
Treatment and study plan
Primary outcomes
-
Utrine rupture Bladder injury
Time frame: 1year
Study contacts
Contact information is provided by the study sponsor or research team.
Diaa El- Din Mohamed Abdel -Aal, Professor
CONTACT
Hwayda Refaat Sayed, Lecturer
CONTACT
+20
Sponsors and collaborators
Lead sponsor
Assiut University
Other
Registry information
Important dates
- Study start
- 2026
- Primary completion
- 2027
- Study completion
- 2027
- First posted
- Apr 13, 2026
- Registry last updated
- Apr 13, 2026
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.