comparative study of PEC block and Erector spinae block in patients undergoing breast surgeries.

Phase 4

• Conditions: Health Condition 1: null- 1. Age 18 to 60 years2. ASA I/II3. Schedule for unilateral MRM

• Registration Number: CTRI/2017/11/010569
• Lead Sponsor: All India Institute of Medical Sciences Patna

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

18 to 60 years female patients, ASA status I/II who are Scheduled for unilateral MRM

Exclusion Criteria

Patients with ASA status III or more, Patients with psychiatric disorder, those having Pre-existing neurological disease, Patients not willing to give consent, having BMI > 40.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of analgesia (time to first rescue analgesia after administration of block) & total analgesic consumption in 24 h after surgery. <br/ ><br>Timepoint: 1st rescue analgesic will be given when VAS Score is more than or equal to 3 which will be assessed at 0.5,1,2,4,6,8,12,24 hours post-operatively.

Secondary Outcome Measures

Name	Time	Method
Postoperative pain (VAS score), Sensory level achieved & Adverse effects if any. <br/ ><br>Timepoint: VAS Score will be assessed at 0.5,1,2,4,6,8,12,24 hours post-operatively. Sensory dermatomal level will be assessed after 30 minutes of block. adverse effect will noted if occurs any time post-operatively.