A comparative study of two types of pain relieving nerve blockade techniques(erector spinae block and pectoral nerve block) in terms of pain relief during and after surgery, and the comfort level of patients while performing the nerve blockade procedure in patients undergoing breast cancer surgery
Phase 4
- Conditions
- Health Condition 1: - Health Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2023/09/057261
- Lead Sponsor
- Dr Anita Sharma
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA Physical status I and II.Undergoing modified radical mastectomy under general anaesthesia
Exclusion Criteria
Infection at the block site.
Allergy to local anaesthetics.
Decreased cardiac and pulmonary reserve.
renal dysfunction.
Any psychiatric condition.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine & compare the duration of post-operative analgesia.The duration will be taken as time from institution of block till the requirement of rescue analgesia.Timepoint: Patients will be assesed for pain using VAS scale after every 2 hours till 12 hours & then every 4 hours till 24 hours postoperatively.
- Secondary Outcome Measures
Name Time Method 1.To determine patient procedure comfort level with grading from 0 to 3 where 0 means anxious & uncomfortable & feeling pain throught the procedure.1means anxious and feeling uncomfortable during needle manipulation.2 means relaxed and comfortable during the procedure but anxious about the outcome.3means relaxed and comfortable throughout the procedure and positive about the outcome.2 To assess patient satisfaction score after 24 hours of block placement.This will be grade as 0 means not satisfactory.1means neutral.2means satisfactory3means optimal patient will recommend the procedure to fellow patients.Timepoint: 3.Total number of rescue analgesia in the form of injection tramadol consumed in first 24 hours.