Study comparing the effect of pain relief provided by one combination of drug(Ketofol) with that of the other(Etofen)
Phase 1
Completed
- Conditions
- Health Condition 1: T14-T14- Injury of unspecified body region
- Registration Number
- CTRI/2019/01/017329
- Lead Sponsor
- Department of Emergency Medicine Bangalore Baptist Hospital Bellary road Hebbal Bangalore
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 108
Inclusion Criteria
All patients who decided to receive PSA for procedures and ASA physical status 1 or 2
Exclusion Criteria
1)Hypersensitivity to Ketofol or Etofen 2)Age less than 18 years 3)ASA 3 and 4
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method