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Comparison of propofol and Ketofol for better hemodynamics in laparoscopic cholecystectomy- A prospective randomized control study

Hemodynamic changes following administration of propofol and ketofol as induction agents in laproscopic surgery under general anaesthesia A prospective randomized control study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/081440
Enrollment
62
Registered
2025-02-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: GROUP KF: Ketofol: Injection Propofol 1 mg/kg plus Injection Ketamine 1 mg/kg diluted to 20 ml normal saline in a syringe for induction of anaesthesia to be given till the loss of eyela

Sponsors

B.J. Medical college and civil hospital Ahmedabad
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Elective laparoscopic surgery under general anaesthesia ASA Grades I, II, III Age 18 60 years

Exclusion criteria

Exclusion criteria: Patient giving negative consent Difficult airway ASA Grade IV,V Cardiopulmonary diseases, hypotension and shock Head injury and neurosurgery Allergic to propofol(egg) and ketamine

Design outcomes

Primary

MeasureTime frame
To compare Hemodynamic parameters (Heart rate, Systolic blood pressure, Diastolic blood pressure, Mean arterial pressure)Timepoint: every 5 minutes till 10 minutes and then every 15 minutes till surgery lasts.—

Secondary

MeasureTime frame
To compare incidence of pain on injection of induction agent.Timepoint: To observe the pain at time of induction.;To compare the incidence of postoperative nausea and vomiting. Timepoint: To observe immediately, then every two hour for 6 hours after extubation.—

Countries

India

Contacts

Public ContactDr Jeel Akbari

B.J. Medical college, Ahmedabad

dhimaraditi@yahoo.in9825334605

Outcome results

None listed

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