A study to investigate a blood test (Arterial lactate) to predict complications (DCI/Vasospasm) and poor prognosis in patient with aneurysmal SAH.
Not Applicable
- Conditions
- Health Condition 1: I609- Nontraumatic subarachnoid hemorrhage, unspecified
- Registration Number
- CTRI/2022/09/045806
- Lead Sponsor
- SCTIMST
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Consenting Adult patients (Caregivers in-case of incapacitated patients) with aSAH admitted at SCTIMST
-Age group 18 years and above (with both sexes included)
-Anterior Circulation Bled Aneurysms
Exclusion Criteria
-Patients/caregivers not consenting for participation in the study.
-Patients with history of Heart Failure/Renal failure/Liver Failure/Shock/Alcoholism/Malignancy -Patients with known congenital errors of Metabolism -Patients on antiretrovirals (NRTI)/Metformin/ Salicylates/beta-adrenergic agonists
-Pregnant/Nursing mothers
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To study serial arterial blood lactate levels in patients presenting with aSAH and check for any correlation between its levels and time to onset of DCI and incidence of DCI.Timepoint: Time to occurrence of Vasospasm or DCI
- Secondary Outcome Measures
Name Time Method To check for any correlation between arterial lactate levels and other outcome parameters.Timepoint: Time to discharge from Hospital