NCT07525362尚未招募不适用
Short Interpregnancy Interval After One Prior Cesarean Delivery and Risk of Intraoperative Maternal Morbidity
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 80
- 主要终点
- Utrine rupture Bladder injury
研究概览
简要总结
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.
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Cross Sectional
入排标准
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Pregnant women with history of one previous cesarean delivery Women admmitted for delivery by cesarean delivery during the study period Singleton pregnancy
排除标准
- •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
结局指标
主要结局
Utrine rupture Bladder injury
时间窗: 1year
次要结局
未报告次要终点
研究者
相似试验
尚未招募
不适用
Evaluation of recovery from caesarean section in pregnant patients.CTRI/2023/12/060428All India Institute of Medical Sciences Jodhpur250
招募中
不适用
A Study for Assessing the Expected and Actual Pain of Back Injection in Pregnant Women Undergoing Caesarean DeliveryCTRI/2025/01/078959SRM Medical College Hospital and Research Centre40
招募中
不适用
Effects of Multi-strain Bacillus Spore Probiotics on Growth, Digestive Function, and Gut Microbiota in Cesarean-Delivered NeonatesNCT07320287Anabio R&D180
Unknown
不适用
请联系我们上传伦理审批文件。 Perinatal outcomes in a subsequent pregnancy among women who have a history of recurrent miscarriageChiCTR2000039588Reproductive Medicine Team20,000
招募中
不适用
The Effect of the Cesarean ERAS Protocol on Mother-Infant and Father-Infant Bonding: a Multicenter, Randomized Controlled Clinical Trial.NCT07276126Okan University1
