Effectiveness of Ketofol versus Propofol Induction on Hemodynamic Profiles in Adult Elective Surgical Patients: - A Double Blind Randomized Controlled Trial.
Phase 1
Not yet recruiting
- 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
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie Ketofol's hemodynamic effects compared to Propofol in adult surgical patients?
How does Ketofol compare to standard-of-care Propofol in hemodynamic stability during anesthesia induction?
Are there specific biomarkers that predict differential response to Ketofol versus Propofol in elective surgery?
What are the known adverse events associated with Ketofol use in clinical anesthesia settings?
What combination therapies or alternative anesthetics show similar hemodynamic profiles to Ketofol in adult patients?