Evaluating the efficacy of Ultrasound guided TAP block for post operative analgesia post Caesarean sectio

Not Applicable

• Conditions: Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium

• Registration Number: CTRI/2021/02/031022
• Lead Sponsor: Sri Ramachandra Institute of Higher Education and Research

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Patients with singleton pregnancy, undergoing Elective Caesarean section under spinal anesthesia

Patients belonging to ASA grade 2.

Exclusion Criteria

Patient refusal

Age <18 years

Age >40years

BMI >35 kg/m2

Allergy to local anesthesic agents

Emergency Caesarean section

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Time to initial onset of pain at the incision site (VAS score above 4). <br/ ><br> <br/ ><br>Total amount of Inj.Tramadol at the end of 24 hrsTimepoint: 0 minute, 30 minutes, 1st, 2nd, 4th,8th, 12th, 16th, 20th and 24th hour. <br/ ><br> <br/ ><br>Total amount of Inj.Tramadol at the end of 24 hrs

Secondary Outcome Measures

Name	Time	Method
Pain score <br/ ><br>Nausea score <br/ ><br>Sedation score <br/ ><br>Patient satisfaction scoreTimepoint: 0 minute, 30 minutes, 1st, 2nd, 4th,8th, 12th, 16th, 20th and 24th hour.