eurological outcome in Polytrauma patient having traumatic brain injury coming for non neurosurgery under BIS and Non-BIS guided anaesthesia : A Randomised Controlled Study.
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/07/055403
- Lead Sponsor
- Department of Anaesthesia and Intensive Care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
1.Polytrauma patient with Traumatic brain injury of age 18-60 year coming for emergency non neurological surgery in less than 7 days post injury.
2.Patients or their relatives giving consent to participate in the study
1.Polytrauma patient not within the described age limit.
2.Baseline BIS value less than 60
3.Forehead injury where BIS monitor cannot be placed.
4.Perioperative hypothermia.
5.Dyselectrolytemia.
6.Patients not requiring general anaesthesia.
7.Patients or relatives not giving consent
8.Pregnant patient
9.Spine surgery
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess postoperative neurological outcome by using FOUR score between BIS guided & non-BIS guided anaesthesia depth monitoring in Traumatic brain injury patient undergoing emergency non neurosurgical surgery.Timepoint: 72 hours postsurgery
- Secondary Outcome Measures
Name Time Method To compare FOUR score & GCS post-surgery. <br/ ><br> To compare GOS-E. <br/ ><br>Timepoint: FOUR Score & GCS at 24hours postsurgery. <br/ ><br> <br/ ><br>GOS-E after 3months postsurgery telephonically <br/ ><br>