Comparing two different pain reducing modalities following propofol injectio
Not Applicable
- Registration Number
- CTRI/2022/12/048300
- Lead Sponsor
- All India Institute of Medical Sciences Patna
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA status : I and I
BMI : 18.5 â?? 34.9 kg/m2
Patients posted for elective surgery of 120 minutes duration.
Exclusion Criteria
Refusing to sign consent
BMI > 35
Pregnant, breast feeding women
ASA status : III-IV
History of alcohol and drug abuse
History of psychiatric illness
Contraindications or allergy to study drugs
Inability to comprehend pain.
Difficult IV cannulation
Difficulty in communicating
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the intensity of pain on propofol injection after the use of Low dose ketamine and Pressure Vibration Mechanical device with placebo using McCrirrick and Hunter verbal rating score.Timepoint: 5 minutes
- Secondary Outcome Measures
Name Time Method To compare the Baseline, Pre-induction and Post-induction hemodynamic parametersTimepoint: 5 minutes;To compare the patientâ??s recall of Pain Perception and Willingness to receive the either of the modalities to prevent pain on propofol injection during the next surgical procedure or examination requiring Propofol injectionTimepoint: 5 minutes;To record any adverse events.Timepoint: 5 minutes