Study to compare hemodynamic stability and analgesia in patients recieving Propofol -Fentanyl Vs Propofol -Ketamine combinatio
Phase 3
- Conditions
- Health Condition 1: R688- Other general symptoms and signs
- Registration Number
- CTRI/2024/02/062339
- Lead Sponsor
- Guru Gobind Singh Medical College and Hospital Faridkot
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients from 18-60years of age scheduled for elective surgeries of 30-90 mins duration and belonging to ASA Grade I and II
Exclusion Criteria
Patients who are hemodynamically unstable
History of anaphylaxis or allergy to the study drugs
Pregnant females
History of head injury or seizure disorders
Psychiatric illness or drug abuse
BMI more than equal to 30 kg per metre square
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare hemodynamic stability of Propofol-Fentanyl Vs Propofol -Ketamine combination in elective short surgical proceduresTimepoint: To compare hemodynamic stability of Propofol-Fentanyl Vs Propofol -Ketamine combination in elective short surgical procedures of 30-90 minutes duration over a period of 1.5 years
- Secondary Outcome Measures
Name Time Method To compare analgesia in patients recieving Profol-Fentanyl Vs Propofol -Ketamine combination in elective short surgical procedures of duration 30 to 60 minutesTimepoint: Outcome will be assessed at the end of one & half year of study