MedPath

Comparative study of brain function monitoring and proactive brain protection for neurologic outcome in patients undergoing brain aneurysm surgery

Not Applicable
Conditions
Health Condition 1: G94- Other disorders of brain in diseases classified elsewhere
Registration Number
CTRI/2019/10/021496
Lead Sponsor
ational Institute of Mental Health and Neurosciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

a) Patients requiring temporary parent vessel occlusion, during surgical clipping of ruptured intracranial aneurysm of anterior circulation

Exclusion Criteria

a)Previous intracranial or spinal surgery

b)Previous stroke or coronary event

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
a)Difference of incidence of new onset neurological deficit within 24 hours postoperatively, between the groupsTimepoint: Within 24 hours after surgery
Secondary Outcome Measures
NameTimeMethod
a)Difference of neurological outcome between the groups as measured by Extended Glasgow Outcome Scale (GOSE)Timepoint: 3 months, 6months
© Copyright 2025. All Rights Reserved by MedPath