Comparative study of Etomidate and Propofol for anesthesia in patients with Cervical compression and deranged Heart rate variability
Not Applicable
- Conditions
- Health Condition 1: G55- Nerve root and plexus compressionsin diseases classified elsewhere
- Registration Number
- CTRI/2021/01/030207
- Lead Sponsor
- Dr Geetha
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
patients aged 18 to 70 years, ASA 1 to 3, with history of cervical myelopathy, presenting for elective anterior or posterior cervical decompression with or without fusion.
Exclusion Criteria
1.Patients with heart rate or rhythm abnormalities
2.Re exploration procedures and patient in sepsis/recovered from sepsis
3.Diabetic patients
4.Degenerative neurological disease
5.Complete spinal cord injury
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Hemodynamic fluctuationsTimepoint: . The Heart rate and Blood pressure will be recorded and noted at Baseline, at induction, at laryngoscopy, and 1, 3, 5, 10 mins post intubation
- Secondary Outcome Measures
Name Time Method Incidence of pain at injection and any myoclonic movements will be recordedTimepoint: At the time of injection