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Sugar levels of blood during brain tumour surgeries while under propofol,sevoflurane and desflurane anaesthesia

Plasma glucose levels in patients undergoing surgery for supratentorial gliomas. A comparison between Sevoflurane, Desflurane and Propofol based anaesthetic regimens

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2019/04/018609
Enrollment
90
Registered
2019-04-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: - Health Condition 2: M511- Thoracic, thoracolumbar and lumbosacral intervertebral disc disorders with radiculopathy

Interventions

None listed

Sponsors

None
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I and II patients

Exclusion criteria

Exclusion criteria: 1 Patient refusal 2 Pregnant or lactating patients. 3 Patients with psychiatric disorders/behavioral impairment or on antipsychotic drugs 4 Patients with significant diabetes, thyroid dysfunction, hepatic, cardiovascular,pulmonary or renal disorders 5 Morbid obesity 6 Patients with allergy to study drugs or history of malignant hyperthermia 7 Chronic drug/alcohol abuse 8 Patients taking steroids, beta adrenergic blocking agents, insulin or oral hypoglycaemic agents.

Design outcomes

Primary

MeasureTime frame
1) To compare the intraoperative plasma glucose levels in patients undergoing craniotomy for supratentorial glioma under general anaesthesia using sevoflurane, desflurane or propofol based regimens during different stages of the surgeryTimepoint: 1)Sample collected prior to induction and hourly thereafter till the completion of surgery

Secondary

MeasureTime frame
1) To compare the incidences of postoperative complications like headache, giddiness, nausea, vomiting or pain at injection sites 2)To compare the time taken by subjects administered these three anaesthetic regimens to achieve a modified Aldreteâ??s Score of 9. 3) To compare the satisfaction of the patients regarding the quality of anaesthesia. Timepoint: 1) Within 24 hours of surgery 2) Hours sfter extubation 3) After 24 hours of surgery

Countries

India

Contacts

Public ContactRudrashish Haldar

Dept. of Anaesthesiology,SGPGIMS, Lucknow

rudrashish@yahoo.com9256543256

Outcome results

None listed

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