Comparative evaluation of analgesic efficacy of different concentrations of Levobupivacaine In Ultrasound Guided Erector Spinae Block For Breast Surgery
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- TOTAL DURATION OF ANALGESIA WILL BE NOTED IN TWO GROUPS POSTOPERATIVELY .IT WILL BE TAKEN FROM TIME OF COMPLETION OF INJECTION TO THE REQUEST OF FIRST RESCUE ANALGESIA
Study Overview
Brief Summary
total of 60 patients will be randomly allocated into 2 study groups of 30 patients each .Each group will receive erector spinae block before induction with general anesthesia technique .Group A will recevie 20ml of 0.25%levobupivacaine and Group B will receive 20ml of 0.375% levobupivacaine . Duration of postoperative analgesia in first 24 hours postoperatively will be noted and compared .After completion of study ,observation obtained will be tabulated and analysed using appropriate stastical methods. .
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Study Design
- Study Type
- Interventional
- Allocation
- Computer generated randomization
- Masking
- Not Applicable
Eligibility Criteria
- Ages
- 20.00 Year(s) to 65.00 Year(s) (—)
- Sex
- Female
Inclusion Criteria
- •ASA I AND II PATIENTS PATIENTS SCHEDULED FOR BREAST SURGERY.
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
TOTAL DURATION OF ANALGESIA WILL BE NOTED IN TWO GROUPS POSTOPERATIVELY .IT WILL BE TAKEN FROM TIME OF COMPLETION OF INJECTION TO THE REQUEST OF FIRST RESCUE ANALGESIA
Time Frame: In the first 24 hours of postoperative period
Secondary Outcomes
- QUALITY OF ANALGESIA(in postoperative period at 0,2‚4‚8‚12‚18‚24hours)
