Assessment of the efficacy of ultrasound guided erector spinae plane block for postoperative analgesia in thoracolumbar spinal surgeries
Phase 3
Recruiting
- Conditions
- Anaesthesia
- Registration Number
- PACTR201910691333405
- Lead Sponsor
- Faculty of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 22
Inclusion Criteria
ASA 1-3 patients scheduled for lower thoracic or lumbar spinal surgery
Age 18-65 years
Sex: Both male and female
Exclusion Criteria
Patient with chronic pain syndrome
Patients on long term opioids.
History of allergy to local anaesthetics
Recurrent back surgeries
Chronic Kidney disease
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post operative morphine consumption in milligrams for the first 24 hours after surgery, compared to the consumption of the control group to assess if the intervention will reduce the opioid needs in thorasic and lumbar spine surgery.Pain will be assessed using the visual analogue scale.
- Secondary Outcome Measures
Name Time Method Visual Analogue Scale will be assessed directly postoperative and then every 6 hours till the end of the first 24 hours after surgery.<br>;First analgesic request<br>