A clinical trial to study the effect of an additional procedure named basal cisternostomy in head injury patients planned for decompressive craniectomy
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/04/042144
- Lead Sponsor
- King Georges Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
Patients of age 18 years and above presenting with traumatic brain injury having surgically evacuable lesions and brain is bulging after evacuation of hematoma.
Exclusion Criteria
1. Hemodynamic instability (polytrauma cases)
2. Pregnant females
3. Coagulopathy
4. Brain stem dysfunction and signs of irreversible brain damage (b/l fixed dilated pupils)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To study intracranial pressure in post operative periodTimepoint: 72 hours
- Secondary Outcome Measures
Name Time Method GCS/GOS at 6 weeks/12 weeksTimepoint: 6 weeks/ 12 weeks;Mid line shift and status of basal cisterns in CT in post op period/on 3rd day post operative /on 7th day post opTimepoint: Postoperative Day 1, Day 3 & Day 7;Mortality within one week/2 weeks/3 weeks (related to TBI sequelae)Timepoint: one week, two weeks & 3 weeks.;No of days on ventilator/ in ICU <br/ ><br>Timepoint: No of days on ventilator/ in IC