Recovery in planned neurosurgery in a group of patients
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/04/066005
- Lead Sponsor
- SIMS Hospitals
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 1 and 2, patients admitted for elective craniotomy for a single intracranial supratentorial lesion
Exclusion Criteria
ASA 3 and 4, patients with major comorbid conditions, obese individuals with BMI more than or equal to 30, patients with drug allergies or egg allergy, patients participating in any other clinical studies, patient with major neurological deficits
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of hospital stay and total hospitalisation costTimepoint: From admission to discharge
- Secondary Outcome Measures
Name Time Method Readmission rates, postoperative complications, postoperative pain scores, perioperative opioid consumption, length of ICU , duration of drainage tube, time to first oral intake, postoperative functional recovery statusTimepoint: 30 days from day of discharge