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The study of effect on the electrical impulses generated by brain when either two of the anaesthetic drugs (propofol or ketofol) is used to maintain anaesthesia in patients who are undergoing surgery for cerebello pontine angle tumours

Effect of Propofol versus Ketofol Infusion on Transcranial Motor Evoked Potentials in Patients Undergoing Cerebellopontine Angle Tumour Surgeries- A Prospective Randomised Blinded Clinical Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070198
Enrollment
70
Registered
2024-07-08
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

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: Propofol Infusion: During the conduct of motor evoked potential monitoring, anaesthesia is maintained by using propofol infusion in the first group Control Intervention1: Ketofol Infusi

Sponsors

Sanjay Gandhi Post Graduate Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anaesthesiologists Class I or II patients Adult Patients with BMI less than 30

Exclusion criteria

Exclusion criteria: Patients unable (legally incompetent) or unwilling to give consent. Previous history of psychiatric, anxiety or post-traumatic stress disorders. History of allergy to study drugs. Patient on sedative or hypnotic medication. Patients with chronic pain or on painkiller. Patients with severe hepatic or kidney disorders. Patients having a history of thyrotoxicosis or cardiac disorders. Patients on chronic beta blockers.

Design outcomes

Primary

MeasureTime frame
Compare the effect of Propofol and Ketofol on amplitude and latency of Transcranial Motor Evoked Potentials when these agents are used with Fentanyl for the maintenance of general anaesthesia in cerebellopontine angle tumour surgeriesTimepoint: Amplitude and latency to be recorded every 30 minutes for the first 3 hours of surgery followed by every hour till the end of surgery

Secondary

MeasureTime frame
1.Comparison of hemodynamic intraoperative parameters between the two anaesthetic regimens every 30 minutes for the first 2 hours then every hour till the end of surgery. 2.Complications like nausea vomiting, pain at injection site, nystagmus, agitation, hallucinations etc Timepoint: 1. Every 30 minutes for the first 3 hours of surgery followed by hourly till the end of the surgery 2. After extubation of the patients which is usually 12 hours after surgery

Countries

India

Contacts

Public ContactTwarita Singh

Sanjay Gandhi Post Graduate Institute of Medical Sciences

rudrashish@yahoo.com9256543256

Outcome results

None listed

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