Assessing pain relief after the operation after administering the pain killer injection during operation according to measurement done (SPI) using special monitor.
Phase 4
- Conditions
- Health Condition 1: null- Patient undergoing Lumbar Laminectomy and Discectomy surgery
- Registration Number
- CTRI/2018/02/012150
- Lead Sponsor
- SDM College of Medical Sciences and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)Patients undergoing elective lumbar spine surgeries
2)ASA I and ASA II patients
3)patients who have given written consent to
participate
Exclusion Criteria
1)patient refusal
2)autonomic neuropathy
3)patient with cardiac arrhythmias
4)presence of a pacemaker
5)medication with anticholinergic drugs,
ketamine or clonidine, Beta-blockers
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method