Comparison of the pain relieving effect of two approaches to the ultra-sound guided back muscle in patients undergoing breast operatio
Not Applicable
- Conditions
- Health Condition 1: C509- Malignant neoplasm of breast of unspecified site
- Registration Number
- CTRI/2023/11/059468
- Lead Sponsor
- All India 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
a) ASA I- II
b) Scheduled to undergo elective modified radical mastectomy
Exclusion Criteria
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.Timepoint: Post-operative period at 0, 0.5, 1, 2, 4, 6, 12 & 24 hours
- Secondary Outcome Measures
Name Time Method 24-hour fentanyl consumptionTimepoint: 1st 24 hours of post-operative period;Intraoperative opioid consumption.Timepoint: Intraoperative period; ? Incidence of adverse events (postoperative nausea/ vomiting, respiratory depression, pruritus, urinary retention) retention)Timepoint: 1st 24 hours of post-operative period.;Patient satisfaction scoreTimepoint: Post-operative period at 0, 0.5, 1, 2, 4, 6, 12 & 24 hours;Time to first analgesic requirement in post-operative period.Timepoint: 1st 24 hours of Post operative period