to compare quality of awakening after anesthesia in patients who recieve normal routine dose versus additional anticonvulsant dose during supratentorial craniotomy.
Phase 4
- Conditions
- Health Condition 1: G998- Other specified disorders of nervous system in diseases classified elsewhere
- Registration Number
- CTRI/2023/06/054486
- Lead Sponsor
- Mahatma Gandhi medical college and hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA physical status I, II, III
Aged 18-60 years scheduled for supratentorial craniotomy for tumor resection
patients who were receiving single anticonvulsant medication for more than one-week duration
Exclusion Criteria
Patient refusal
History of allergy to the study drug
Impaired renal/hepatic function.
Severe left ventricular dysfunction,
Seizures within one week prior to surgery despite the use of antiepileptic drug, patients who were on two anticonvulsants,
Patients with GCS 4 cm associated with midline shift of >5 mm,
surgery lasting longer than 5 hours with >30% blood volume loss
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method