A clinical study to determine the effect of anaesthetics in lower segment caesarean section.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/02/049768
- Lead Sponsor
- BGS Global Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.ASA Physical status II parturients.
2.Parturients undergoing elective lower segment caesarean section using Pfannenstiel incision under subarachnoid blockade.
3.Height of parturient: 150 cms to 170 cms.
4.Weight of parturient 50 kgs to 90 kgs.
Exclusion Criteria
1.Patient refusal or unable to give written informed consent. E.g.: psychiatric patients
2.Patients with known allergy to study drugs
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual Analogue Scale (VAS) scoreTimepoint: Baseline, After subarachnoid blockade, Before TAP block, 0 mins, 30 mins, 1 hour, 2 hours, 4 hours, 6 hours, 8 hours, 10 hours, 12 hours, 16 hours, 24 hours
- Secondary Outcome Measures
Name Time Method Heart rate, Systolic Blood Pressure, Diastolic Blood Pressure, Mean arterial pressure, Room air saturation of oxygen (SpO2), Time to first mobilisation, Time of rescue analgesic use, Side effectsTimepoint: Baseline, After subarachnoid blockade, Before TAP block, 0 mins, 30 mins, 1 hour, 2 hours, 4 hours, 6 hours, 8 hours, 10 hours, 12 hours, 16 hours, 24 hours