Effectiveness of Ketofol versus Propofol Induction on Hemodynamic Profiles in Adult Elective Surgical Patients: - A Double Blind Randomized Controlled Trial.
Phase 1
- Conditions
- Anaesthesia
- Registration Number
- PACTR202008628465772
- Lead Sponsor
- Dilla University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 125
Inclusion Criteria
ASA I and II
-Age 18-65 years
Exclusion Criteria
-Obstetric, Neurosurgical and ENT surgery are excluded
-Those on long time opioid use/ sedative preoperative adjunctive medications
-Those who use psychotropic drugs
-any known contraindications/allergy to ketamine or propofol
-pre-operative anxious patients
-patient in pain
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Our primary endpoints were a change in hemodynamic parameters (MAP, SBP, and HR) from baseline immediately after induction, 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes, and 30 minutes
- Secondary Outcome Measures
Name Time Method Secondary endpoints include postoperative pain, nausea, and vomiting incident was graded and recorded in the PACU.