A clinical trial to study the effect of intermittent pneumatic leg compression on blood pressure after induction of general anaesthesia on patients undergoing sub axial cervical spine surgery
Phase 2
- Conditions
- Health Condition 1: M509- Cervical disc disorder, unspecified
- Registration Number
- CTRI/2024/05/066999
- Lead Sponsor
- Dr Bigyan Chaulagain
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA I to ASA II patients with single level sub axial cervical spine fracture dislocation with neural deficit and no contraindication to leg compression
Exclusion Criteria
Patient refusal, inability to give informed consent, hemodynamically unstable or patients in spinal shock, unstable angina, poor LV function (EF less than 40 percent), arrhythmia requiring treatment, uncontrolled comorbidites and patients with contraindication to pneumatic leg compression such as DVT or peripheral arterial disease
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of post induction hypotension i.e, systolic blood pressure less than 90mmHg after induction of general anaesthesiaTimepoint: From induction of general anaesthesia to 20 minutes after induction
- Secondary Outcome Measures
Name Time Method Arterial Blood Gases in terms of base deficit, lactate and P/F ratioTimepoint: Just after induction, 20 minutes after induction and at skin closure;Incidence of complications of pneumatic leg compressionTimepoint: post operative period;Number of hypotensive episodesTimepoint: Throughout the surgery;Prone positioning related hypotensive eventsTimepoint: After prone positioning (if applicable) and thereafter throughout the surgery;Use of vasopressors and intravenous fluidsTimepoint: first 20 minutes and throughout the surgery