Adverse events following cesarean delivery in mother and child
Not Applicable
- Conditions
- Health Condition 1: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium
- Registration Number
- CTRI/2023/11/059750
- Lead Sponsor
- Vijayanagar institute of medical sciences Contonment ballari
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
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
Exclusion Criteria
1.Patients who refuse to participate in this study
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the incidence of peri operative anaesthesia related maternal adverse events in patients undergoing cesarean delivery.Timepoint: From intra operative period to 24 hours postoperatively after cesarean delivery
- Secondary Outcome Measures
Name Time Method 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 <br/ ><br>2)Assess for correlation with types of anaesthetic drugs, obstetric history, medical history and co-morbidities. <br/ ><br>3)To assess the incidence of anaesthesia related neonatal adverse outcomes in terms of APGAR score at 1 min and 5 mins, umblical cord blood gas analysis, NICU admission <br/ ><br>Timepoint: 1 year