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Comparative study of isoflurane and sevoflurane on recovery profile and; BP and Heart rate changes in patients undergoing neurosurgery

Comparative effect of isoflurane and sevoflurane on recovery profile and hemodynamics in patients undergoing neurosurgery - A Prospective, Parallel group, Observational study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/01/062032
Enrollment
36
Registered
2024-01-30
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: G988- Other disorders of nervous system

Interventions

Intervention1: NA: NA Control Intervention1: NA: NA

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients undergoing intracranial neurosurgery under general anaesthesia and maintained on either isoflurane or sevoflurane 2. American Society of Anaesthesiologist (ASA) grade I or II

Exclusion criteria

Exclusion criteria: 1. Diagnosed patients of pituitary adenoma on CT 2. Previous History of neurosurgery 3. History suggestive of allergies to isoflurane or sevoflurane 4. Patients with comorbidities like Hypertension and Diabetes Mellitus. 5. Pregnant women 6. Patients with history of malignant hyperthermia, preexisting renal insufficiency, Hepatic disease, Endocrine disease, Neurological abnormality and electrolyte abnormalities

Design outcomes

Primary

MeasureTime frame
Recovery end-points were measured as the time from closure of anesthesia to various time intervals of the anaesthetic vaporizer. • Difference in patients achieving recovery profileTimepoint: NA

Secondary

MeasureTime frame
1. Difference in the Blood pressure and Heart Rate of isoflurane and sevoflurane from baseline to various time intervals 2. To assess the safety of isoflurane and sevoflurane in terms of adverse events (alteration of hemodynamics and adverse drug reaction)Timepoint: 1 Blood Pressure and Heart Rates were measured (1hour,2hour,3hour,4hour,5hour) intraoperatively 2 Adverse events were seen perioperatively and postoperatively upto 2 hours

Countries

India

Contacts

Public ContactDr Nikhil Mujbaile

GMCH, Nagpur

chelsycosmos@rediffmail.com8208650362

Outcome results

None listed

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