Analgesic efficacy of ultrasound guidederector spinae fascial plane block in lumbarspine surgeries
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/07/070190
- Lead Sponsor
- All India Institute of Medical Sciences Kalyani
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) ASA I and ASA II
2) Scheduled for elective lumbar spine surgery (PLIF and TLIF)
3)Lumbar spine surgery involving not more than three levels
Exclusion Criteria
1)Patients with pre-existing neurological deficits
2)Patients undergoing emergency or revision lumbar spine surgery
3)Patients with contraindications to erector spinae block
4) Patients with opioid dependence.
5)Patient with scoliosis.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1)Time to first request of analgesia. Postoperative pain scores assessed using Visual Analog Scale (VAS) at 6,12 and 24 hours postoperatively <br/ ><br>2)Total opioid consumption in first 24 hours postoperativelyTimepoint: In first 24 hours postoperatively at 6th hour,12th hour and 24th hour
- Secondary Outcome Measures
Name Time Method 1.Incision response <br/ ><br>2.Surgical field experience <br/ ><br>3.Postoperative nausea and vomiting (PONV) <br/ ><br>4.Time to ambulation post surgery. <br/ ><br>5.Patient satisfaction with postoperative pain management.Timepoint: First 24 hours postoperative