a clinical trial of two different regional block techniques for comparing pain relief efficacy in breast surgeries.
Phase 4
- Conditions
- Health Condition 1: C509- Malignant neoplasm of breast of unspecified siteHealth Condition 2: C501- Malignant neoplasm of central portion of breastHealth Condition 3: C500- Malignant neoplasm of nipple and areolaHealth Condition 4: C00-D49- Neoplasms
- Registration Number
- CTRI/2022/04/042085
- Lead Sponsor
- yenepoya medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
american society of anaesthesiologist grade 1 to 3.
unilateral female breast surgeries.
able to answer verbally.
Exclusion Criteria
inability to consent
bilateral breast surgeries
psychiatric disorders
chronic neurological disease
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method visual analogue scale <br/ ><br>(VAS score) ranging from 1-10Timepoint: POST OPERATIVELE T-0.5 HOURS,T-1HOURS,T-2HOURS,T-4HOURS,T-8HOURS,T-12 HOURS,T-16HOURS,T-24HOURS.
- Secondary Outcome Measures
Name Time Method rescue analgesia requirementTimepoint: in hours as to when rescue analgesia was required to control pain.