Assessing the efficacy of Ketamine and Profopol mixed together in a single syringe to sedate or reduce pain during a procedure in the Emergency Department
Phase 4
- Conditions
- Health Condition 1: null- All trauma patients, between 18 and 60 years of age, with a visual analog scale pain score of more than or equal to 6/10, and require a procedural sedation and analgesia.
- Registration Number
- CTRI/2017/10/010271
- Lead Sponsor
- Department of Emergency MedicineDepartment of Emergency Medicine Sri Ramachandra University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age >18 yrs to <60 yrs
2.For whom the treating physician selected KETOFOL for procedural sedation and analgesia
3.Visual Analog Scale pain score of > 6/10
Exclusion Criteria
1.Hemodynamically unstable patients
2.Patients with respiratory compromise
3.Suspicion of head injury or raised ICP
4.Presence of psychiatric history
5.Chronic respiratory, renal or hepatic failure
6.Pregnant patients
7.Documented allergy to propofol or ketamine
8.Inability to understand VAS pain score
9. Not willing to give a written consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method