A study to know whether dexmedetomidine when added to bupivacaine for ultrasound guided erector spinae block is effective for postoperative analgesia after spine surgery or not?
Not Applicable
- Conditions
- Health Condition 1: M478- Other spondylosis
- Registration Number
- CTRI/2020/08/027180
- Lead Sponsor
- AiimsRishikesh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 1 & 2 patients Scheduled for elective Spine Surgery
Exclusion Criteria
Refusal of consent.
Patients having psychotic disorders.
Patients with poor cognitive functions preoperatively or postoperatively.
Patients intended for postoperative mechanical ventilation or not extubated at the time of surgery.
Patients require reintubation during study period.
Patients with chronic headache or on analgesics for long duration.
Known or suspected allergy to study drugs.
Patients with uncontrolled hypertension, uncontrolled D.M or heart disease.
Patients with heaptic and renal disease.
Asthmatic and immunocompromised Patients.
BMI > 30 kg/m2
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of Analgesia (request for first analgesia) <br/ ><br>Numerical Rating Scale (NRS) pain score at various time points in postoperative period till 24 hours. <br/ ><br>Total Analgesic consumption in intraoperative and post-operative period till 24 hours. <br/ ><br>Timepoint: Baseline ,1,5 mnt after induction,1,5 mnt after block, during,1mnt,5,30 mnt mnt after incision, during 1,5 mnt after closure,
- Secondary Outcome Measures
Name Time Method Change of hemodyanamics (HR, MAP) or any complications intraoperative and postoperative period till 24 hours.Timepoint: 1,2,4,8,12,16,24 hour postextubation