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Comparison of haemodynamic effects of propofol and ketofol as induction agents in general anaesthesia

Comparison of haemodynamic effects of propofol and ketofol as induction agents in patients undergoing discectomy surgeries under general anaesthesia -A prospective randomized double blind study - nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/072316
Enrollment
78
Registered
2024-08-12
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: G55- Nerve root and plexus compressionsin diseases classified elsewhere

Interventions

Intervention1: Ketofol (Ketamine + Propofol): A single intravenous bolus dose of Propofol 1.5mg per kg + Ketamine 0.75 mg/kg diluted to 20ml with normal saline to be given and observed over 30 minutes

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 18-65years American society of Anesthesiologists physical status grade (ASA-PS) I and II Patients requiring GA with endotracheal intubation Patients willing to give the written consent to participate in the study

Exclusion criteria

Exclusion criteria: Patients who are not willing to participate in the study. Patients with uncontrolled hypertension & diabetes mellitus Patients with history of psychiatric illness Patients with history of intolerance or showing anaphylactic reaction to the medications used in the study. Patients with hepatic, renal, cardiac and seizure disorders Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
To compare the Hemodynamic profile (Heart Rate, Systolic Blood Pressure, Diastolic Blood Pressure, and Mean Arterial Pressure) before induction, 1min after induction, 1 min, 3 min, and every 5 min after intubation for a duration of 30 min between the two study groups. Timepoint: 1 min, 3 min, and every 5 min after intubation for a duration of 30 min

Secondary

MeasureTime frame
To compare the recovery time, the need for postoperative rescue analgesia, the incidence of postoperative nausea and vomiting and the level of sedation between the two study groupsTimepoint: every 30mins

Countries

India

Contacts

Public ContactDr Karthik E V N

Sri Venkateswara institute of medical sciences

hemanthn1973@gmail.com9440285634

Outcome results

None listed

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