Adverse events following cesarean delivery in mother and child

Not yet recruiting

• Conditions: 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

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2023-10-11
• Last Update Posted: 2023-10-27

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: Female
• Target Recruitment: 165

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.	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	2)Assess for correlation with types of anaesthetic drugs, obstetric history, medical history and co-morbidities.

Trial Locations

Locations (1)

Vijayanagar institute of medical sciences; 🇮🇳 Bellary, KARNATAKA, India

Vijayanagar institute of medical sciences

🇮🇳Bellary, KARNATAKA, India

Dr Azhaguparvathi a

Principal investigator

9345589871

azhaguab97@gmail.com