Relation of anthropometric measurements with incidence of hypotension in patients undergoing elective LSCS under Spinal Anaesthesia

Not Applicable

Conditions: Health Condition 1: 1- Obstetrics

Registration Number: CTRI/2021/08/035698

Lead Sponsor: Sawai Man Singh Medical College and Hospitals

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: ot Yet Recruiting

Sex: Not specified

Target Recruitment: 0

Inclusion Criteria

Patients willing to give written informed consent

Patients undergoing elective LSCS under spinal anaesthesia

Patients belonging to the ASA Class I and II

Age 20 to 30years

Patients weighing 50 to 80 kg

Height 150 to 160 cm

Exclusion Criteria

Parturient in active labor

Patient allergic to drugs used for spinal anaesthesia

Parturient with placenta previa twin pregnancies oligohydramnios or polyhydramnios gestational hypertension intrauterine growth restriction ruptured membranes

Patients with significant medical or obstetric morbidity

Parturient in obstructed labor abnormal lie or presentation

Patients with any contraindications for spinal anaesthesia

Patients with 3 or more than 3 previous caesarean deliveries

Psychiatric patients

Failed spinal anaesthesia requiring conversion to GA

Study & Design

Study Type: Observational

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Prediction of post spinal hypotension on the basis of independent factors including symphysiofundal height, vertebral column length and abdominal girth in Elective LSCS <br/ ><br>2. Correlation between SFH, VCL and AG with change in haemodynamic parameters (BP,PR). <br/ ><br>Timepoint: 90 mins

Secondary Outcome Measures

Name	Time	Method
1.To estimate the percentage of cases where mean arterial blood pressure decreases by more than or equal to 20% of the baseline value. <br/ ><br>2. To calculate the average dose of vasopressor needed to maintain blood pressure in case of hypotension. <br/ ><br>3. To determine the average level of maximum sensory block achieved. <br/ ><br>4. To determine the correlation between symphysiofundal height, abdominal girth, vertebral column length, height, weight and BMI with the maximum level of sensory block achieved after spinal anaesthesia. <br/ ><br>5. Side effects-nausea, vomiting, shivering if any to be noted. <br/ ><br>Timepoint: 120 mins post operatively