To compare the pain relief provided by thoracolumbar interfascial plane block with the pain relief provided by injecting a large volume of local anaesthetic drug at the site of surgery in patients who underwent spine surgery
Not Applicable
- Conditions
- Health Condition 1: M959- Acquired deformity of musculoskeletal system, unspecifiedHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2021/02/031406
- Lead Sponsor
- Dr Priyanka Pavithran
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients scheduled for Lumbar spine fixation for up to three levels ASA- I, II patients.
2.Age 20 -70 yrs.
3.Body weight between 40-80 Kg
Exclusion Criteria
1.Age <18yr and >70 yrs.
2.Weight <40 Kg and >80 Kg
3.Patients with known allergy to Local anesthetics
4.Revision spine surgery
5.Infection at the site of block
6.Patients on anticoagulants or having bleeding diathesis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method TIME TO FIRST TRAMADOL CONSUMPTIONTimepoint: The time point at which patient requests for tramadol in the postoperative period will be noted in terms of minutes from the point of time the block was administered
- Secondary Outcome Measures
Name Time Method TOTAL DOSE OF TRAMADOL CONSUMED <br/ ><br>BRUGGEMAN COMFORT SCALETimepoint: PACU ADMISSION, 6HOURS,12HOURS,24 HOURS, 48 HOURS POSTOP