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A randomized study to compare the effect of low-dose Ketamine versus Fentanyl on the hemodynamic response to laryngoscopy and endotracheal intubation.

A randomized study to compare the effect of low-dose Ketamine versus Fentanyl on the hemodynamic response to laryngoscopy and endotracheal intubation in Department of Anaesthesiology, SMS Medical College and Attached Hospitals, Jaipur . - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071287
Enrollment
66
Registered
2024-07-25
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: 3- Administration Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Ketamine: 0.5 mg/kg Ketamine intravenously giving only once before 3 minutes of anaesthesia Control Intervention1: Fentanyl: 1 microgram/kg Fentanyl intravenously giving only once befor

Sponsors

SMS Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Elective Surgery under General Anaesthesia Patient willing to give informed and written consent Age group between 18-50 ASA grade 1&2

Exclusion criteria

Exclusion criteria: 1. History of allergy or contraindications of any study drug 2. Patients scheduled for emergency surgery 3. Hypertension - known or previously dignosed 4. Pregnancy 5. Dementia or psychiatric illness 6. Known Ischemic heart disease 7. Raised intracranial pressure or intracranial pathology where a rise in intracranial pressure would pose a risk or patients scheduled for neurosurgical procedures 8. History or indicator of or proven difficult ventilation or laryngoscopy or intubation Intubation time more than 30 seconds or repeated attempts at intubation 9

Design outcomes

Primary

MeasureTime frame
HypertensionTimepoint: At baseline when patient comes to Operation theatre, post induction- within 1 minute of giving induction agent, during laryngoscopy, just after intubation and at 2, 4, 6, 8,10 minutes interval after intubation

Secondary

MeasureTime frame
Tachycardia , post induction hypotension & any side effectsTimepoint: At baseline, post induction, during laryngoscopy, just after intubation & for 10 minutes at 2 minutes interval

Countries

India

Contacts

Public ContactAmbili TP

SMS Medical College

trishala.jain31@gmail.com9414281744

Outcome results

None listed

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