To compare the effect of anesthesia with anaesthetic gas sevoflurane versus isoflurane on blood sugar levels in brain cancer surgeries
- Conditions
- Medical and Surgical,
- Registration Number
- CTRI/2025/03/083071
- Lead Sponsor
- PGIMS Rohtak
- Brief Summary
This study is a prospective double blind randomizedclinical trial. Aim of the study is to compare the c in non diabetic patientsundergoing intracranial mass excision surgery. The objective of the study is tosee the change in hourly blood sugar level trends from baseline, with the intraoperativeuse of inhalational agents; sevoflurane and isoflurane for maintainence.This study is a prospective double blind randomizedclinical trial. Aim of the study is to compare the c in non diabetic patientsundergoing intracranial mass excision surgery. The objective of the study is tosee the change in hourly blood sugar level trends from baseline, with the intraoperativeuse of inhalational agents; sevoflurane and isoflurane for maintainence.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 90
Patients of any sex, non diabetic, ASA status I & II and posted for intracranial mass excision surgery under general anesthesia.
The patients who are diabetic, have disorders of glucose metabolism, are pregnant and lactating , have renal, cardiovascular, pulmonary or hepatic disease, are chronic alcoholic, are taking insulin, oral hypoglycemic agents, antipsychotic drugs and beta adrenergic blocking drugs or are not willing to give consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To note the baseline blood glucose level (before induction) and then the hourly change in intraoperative glucose levels with the use of sevoflurane or isoflurane as a maintenance inhalational agent. Before induction and every hour after induction till completion of surgery
- Secondary Outcome Measures
Name Time Method To note the baseline heart rate, saturation and mean arterial blood pressure and intraoperatively every 2 hour after induction. Before induction and every two hour after induction till completion of surgery
Trial Locations
- Locations (1)
PGIMS Rohtak
🇮🇳Rohtak, HARYANA, India
PGIMS Rohtak🇮🇳Rohtak, HARYANA, IndiaDr Nitu yadavPrincipal investigator8708642484ynitu29@gmail.com