Anaesthesia related maternal and fetal adverse events after cesarean delivery a prospective observational study
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 165
- 试验地点
- 1
- 主要终点
- To assess the incidence of peri operative anaesthesia related maternal adverse events in patients undergoing cesarean delivery.
研究概览
简要总结
Here we are going to observe the rate of anaesthesia related maternal complications and newbornoutcome related to cesarean deliveries.
On arrival to the operating room, basalvital parameters (Heart rate, Blood pressure, Respiratory rate, ECG) will berecorded. Cesarean delivery will be performed under neuraxial or general anaesthesia.The choice of anaesthesia method is determined based on medical history,obstetric history, co-morbidities and contraindications.
Patients will receive standard anaesthesiaas per institutional protocol. The mode of anaesthesia, dose and the drug usedin anaesthesia will be recorded.
The adverse events arehypoxia, desaturation, hypotension, hypocarbia, pain, hypothermia, postoperative nausea and vomiting, need for o2 supplementation, any other form ofventilator support, APGAR score at 1 min and 5 min, umbilical cord blood gasanalysis, NICU admission will be assessed.
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18.00 Year(s) 至 40.00 Year(s)（—）
- 性别
- Female
入选标准
- •1.Patients more than 18 years 2.Patient who is having term pregnancy (37 week) undergoing cesarean delivery in department of VIMS , ballari due to various maternal and fetal indications.
- •3.Patients who categorized as ASA physical status class 2 and above 4.All booked and non-booked patient 5.Patients who are willing to participate will be included in this study after an informed and written consent.
排除标准
- •1.Patients who refuse to participate in this study.
结局指标
主要结局
To assess the incidence of peri operative anaesthesia related maternal adverse events in patients undergoing cesarean delivery.
时间窗: From intra operative period to 24 hours postoperatively after cesarean delivery
次要结局
- 1)To assess the type of anaesthesia related adverse events including hypoxia, desaturation, hypotension, hypocarbia, pain, hypothermia, post operative nausea & vomiting, need for o2 supplementation, any other form of ventilatory support(2)Assess for correlation with types of anaesthetic drugs, obstetric history, medical history and co-morbidities.)