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Comparing the effect of propofol and ketofol on emergence from anesthesia in patients undergoing elective neurosurgery for brain tumours

Comparison of the effect of propofol versus ketofol on emergence from anesthesia in patients undergoing elective supratentorial craniotomy, a prospective randomized double-blind study - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079607
Enrollment
70
Registered
2025-01-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: D496- Neoplasm of unspecified behavior of brain

Interventions

Intervention1: Ketofol infusion for maintenance of anesthesia: Continuous infusion, given intravenously, from start of surgery to end of surgery, at the dose of 0.3 mL/kg/hour Control Intervention1: P

Sponsors

All India Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I & II patients, patients with supratentorial tumor size less than 5 cm, posted for elective craniotomy for tumor excision

Exclusion criteria

Exclusion criteria: Refusal of consent, patients who are expected to need postoperative elective ventilation having massive cerebral edema, midline shift, vascular or high-grade tumor, expected duration of anesthesia greater than eight hours, patients with preoperative GCS less than fifteen, altered sensorium or having aphasia, patients with BMI more than thirty five kg per meter square, pregnant females, patients having psychiatric illness or drug abuse, patients having aphasia, patients requiring post-operative ventilation, patients having history of allergic reactions to study drug, history of previous craniotomy

Design outcomes

Primary

MeasureTime frame
Time for emergenceTimepoint: One point assessment at the end of surgery

Secondary

MeasureTime frame
Heart rate & mean arterial pressure, Intra-operative brain bulge, Time for extubation, Time for recovery, SOMCT in the early postoperative period, Post-operative nausea & vomiting during the early recovery period, Complications of study drugs Timepoint: Intraoperative parameters will be recorded baseline, 5 minutes after intubation, 1 minute after pin insertion completion, 1 minute after skin incision, 1 minute after Dural opening, every 30 minutes intraoperatively, 1 minute after extubation

Countries

India

Contacts

Public ContactBhavna

AIIMS, New Delhi

pandiamihir@gmail.com9013590548

Outcome results

None listed

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