ltrasound guided bilateral block of erector spinae muscle, a muscle in back to reduce pain after traumatic spine surgery
Not Applicable
Completed
- Conditions
- Health Condition 1: M898- Other specified disorders of bone
- Registration Number
- CTRI/2019/03/018206
- Lead Sponsor
- Dr Babita Gupta
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 34
Inclusion Criteria
1. All adults with traumatic spine injury (thoracic/ lumbar spine ) with ASIA grade B to E (i.e with intact sensory function) posted for traumatic spine fixation surgery during the study period.
2. American society of Anaesthesiologist (ASA) grade I/II patients
3. body mass index 20 to 35 kg/m2
Exclusion Criteria
1.Patients refusal
2.Known allergy to local anaesthetic drugs
3.Abnormal back or spine anatomy
4.Infection at the injection site
5.Pregnancy
6.Incision involving more than 6 intervertebral spaces
7.Altered coagulation profiles( PTINR >1.5, platelet count <100,000/cmm)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 24 hours opioid consumption (time frame: 24 hours from injection)Timepoint: 24 hours opioid consumption (time frame: 24 hours from injection)
- Secondary Outcome Measures
Name Time Method 1. Pain score ( time frame : 24 hour postoperative at regulsr intervals 0,3,6,12,18 and 24 hours) <br/ ><br>visual analog scores postoperative pain (0-10) <br/ ><br>2. Time of first analgesic dose <br/ ><br>3.Postoperative nausea and vomiting <br/ ><br>4.Extent of sensory blockade anterior and posteriorly in the immediate postoperative period.Timepoint: 24 hours