Health Condition 1: null- 1. Age 18 to 60 years 2. ASA I/II 3. Schedule for unilateral MRM
Conditions
Interventions
Intervention1: Group 1 patients will receive Erector Spinae block
Group 2 patients will receive PECSI/II block.
: The blocks will be performed under all aseptic precautions in the pre-operating room 3
80 mm) using the same ultrasound machine (Sonosite, Inc., Bothell, WA, USA) and linear array probe (38 mm, 7â??12 MHz frequency). For Erector Spinae Block
20 mls
Sponsors
All India Institute of Medical Sciences Patna
Eligibility
Inclusion criteria
Inclusion criteria: 18 to 60 years female patients, ASA status I/II who are Scheduled for unilateral MRM
Exclusion criteria
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of analgesia (time to first rescue analgesia after administration of block) & total analgesic consumption in 24 h after surgery. 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
| Measure | Time frame |
|---|---|
| Postoperative pain (VAS score), Sensory level achieved & Adverse effects if any. 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. | — |
Countries
India
Contacts
Public ContactDr Chandrakant Prasad
All India Institute of Medical Sciences, Patna
Outcome results
None listed