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Comparing two different pain reducing modalities following propofol injection

Comparing the effect of Low dose Ketamine and Pressure vibration Mechanical device with placebo in preventing pain on propofol injection in patient undergoing elective surgery: A double-blind, Randomised Control study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/12/048300
Enrollment
300
Registered
2022-12-20
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Drug : Ketamine: Route: Intravenous Volume : 5 ml Strength: 50mcg per kg diluted in 0.9% Normal Saline Duration: over 1 minute Frequency : Single shot Intervention2: Pressure Vibration

Sponsors

All India Institute of Medical Sciences Patna
Lead Sponsor

Eligibility

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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—

Countries

India

Contacts

Public ContactNeeraj Kumar

All India Institute of Medical Science Patna

neeraj.jlnmc@gmail.com8210104972

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026