Comparing the efficacy of pain reduction between 2 different injections ( costotransverse foramen block versus thoracic paravertebral block ) over the back in patients undergoing breast surgery.
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/08/044943
- 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
1.Patients undergoing breast surgery under general anaesthesia
2.Patients between 18-70 years
Exclusion Criteria
1.Patient refusal to participate.
2.Known hypersensitivity to local anaesthetic and opioids.
3.Patient having an infection at the site of block.
4.Patient having spinal deformities and previous history of spine surgery.
5.Patients on anticoagulation therapy.
6.Patients with untreated psychiatric illness
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Total analgesic requirements (cumulative morphine consumption )Timepoint: First 24hrs after suregry in PACU.
- Secondary Outcome Measures
Name Time Method 1.11-point NRS scores at rest and at movement in postoperative period at the time interval of 2 hours, 4 hours, 6 hours,12 hours and 24 hours. <br/ ><br>2.Duration of analgesia (time for the first analgesia injection in postoperative period). <br/ ><br>3.Postoperative nausea and vomiting at 2 hours, 4 hours, 6 hours, 12 hours and 24 hours. <br/ ><br>4.Adverse events in 24 hours <br/ ><br>5.Patient satisfaction score. <br/ ><br> <br/ ><br>Timepoint: 1.To assess the post-operative pain using NRS scale at 2 hours , 4 hours , 6 hours , 12 hours and 24 hours. <br/ ><br>2.Postoperative nausea and vomiting at 2 hours , 4 hours , 12 hours and 24 hours. <br/ ><br>3.Adverse events in 24 hours.