Comparative study for post operative analgesic efficacy in breast carcinoma surgery patients
Phase 1
- Conditions
- Health Condition 1: C509- Malignant neoplasm of breast of unspecified site
- Registration Number
- CTRI/2024/01/061422
- Lead Sponsor
- Armed Forces Medical College. Pune
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1). American society of anaesthesiologists- Physical standards classification (ASA-PS) class II And class III individuals.
Exclusion Criteria
1).Patient refusal
2).Age below 18 years and above 65 years
3).ASA-PS Class IV and above
4).Patient with known allergies to any drugs used
5).Local Infection at the site of block
6).Patients receiving opioids for chronic analgesic therapy
7).Inability to comprehend Visual Analogue scale
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of Analgesia and request for rescue analgesiaTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Visual Analogue score of pain and incidence of post operative nausea and vomitingTimepoint: Time frame of 2 hours 4 hours 6 hours 12 hours ad 24 hours