evaluating the effects of propofol in brain using advanced imaging
Phase 3
Completed
- Conditions
- Health Condition 1: null- chronic back pain
- Registration Number
- CTRI/2016/03/006720
- Lead Sponsor
- IMHANS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
patients with chronic back pain
Exclusion Criteria
structural brain pathology
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method BOLD signal changes on fMRITimepoint: pre and post propofol, 6 minutes
- Secondary Outcome Measures
Name Time Method Cardiorespiratory changesTimepoint: Every 5 minutes from baseline till patient is awake