Comparison of the pain relieving effect of two approaches to the ultra-sound guided back muscle in patients undergoing breast operation
- Conditions
- Malignant neoplasm of breast of unspecified site,
- Registration Number
- CTRI/2023/11/059468
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Breast Surgery is associated with significant peri-operative pain and chronic pain. Various pain management modalities have been tried to alleviate the pain, erector spinae plane block is one of them. Recently a cadaveric study has shown two new approaches of erector spinae plane block namely "Erector Spinae Plane Block between Transverseprocesses (BTWN)" and "Erector Spinae Plane Block at medial transverse process(MED)". We wish to compare the efficacy of these two approaches of erector spinae plane block, its analgesic efficacy, its effect on perioperative opioid consumption, patient satisfaction and side effects.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Female
- Target Recruitment
- 60
a) ASA I- II b) Scheduled to undergo elective modified radical mastectomy.
a) Patient refusal for regional techniques b) All contra-indications to regional techniques: Local or systemic infection Known allergy to the study drugs Bleeding disorders Platelet count <80,000/μL of blood c) BMI > 35 d) Inability to use PCA device post operatively.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Efficacy of analgesic technique determined by 11-point numeric rating scale (NRS) at rest & on abduction of ipsilateral arm above the head. Post-operative period at 0, 0.5, 1, 2, 4, 6, 12 & 24 hours
- Secondary Outcome Measures
Name Time Method Intraoperative opioid consumption. Intraoperative period 24-hour fentanyl consumption 1st 24 hours of post-operative period Time to first analgesic requirement in post-operative period. 1st 24 hours of Post operative period Patient satisfaction score Post-operative period at 0, 0.5, 1, 2, 4, 6, 12 & 24 hours ï¬Incidence of adverse events (postoperative nausea/ vomiting, respiratory depression, pruritus, urinary retention) retention) 1st 24 hours of post-operative period.
Trial Locations
- Locations (1)
AIIMS Hospital
🇮🇳South, DELHI, India
AIIMS Hospital🇮🇳South, DELHI, IndiaKunal AggarwalPrincipal investigator8168973866aggarwalkunagupta@gmail.com