A study to evaluate the efficacy of a particular type of anesthesia to provide pain relief following spine surgery.
Not Applicable
- Conditions
- Health Condition 1: S320- Fracture of lumbar vertebra
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
40 ASA (American Society of Anesthesiologists) I-II patients scheduled to undergo lumbar spine surgery under general anesthesia will be enrolled in the study.
Exclusion Criteria
Local infection at the block site
Coagulopathy
Morbid obesity (BMI >40)
Allergy to local anaesthetics
Uncontrolled hypertension or Ischemic heart disease
Renal dysfunction
Pre-existing neurological deficits
Psychiatric illness
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare cumulative analgesic consumption in 24 postoperative hours(morphine)Timepoint: 24 postoperative hours
- Secondary Outcome Measures
Name Time Method Reduction in postoperative pain <br/ ><br>Time to first rescue analgesia <br/ ><br>Adverse effects <br/ ><br>Patient satisfactionTimepoint: 24 postoperative hours