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Noninvasive Assessment of Cerebral Oxygenation and Cardiac Function in Patients With Neurovascular Diseases

Completed
Conditions
Subarachnoid Hemorrhage, Aneurysmal
Registration Number
NCT02991157
Lead Sponsor
National Institute of Mental Health and Neuro Sciences, India
Brief Summary

This prospective observational study will assess the regional cerebral oxygen saturation and cardiac output non-invasively in patients with subarachnoid hemorrhage during nimodipine administration for the prevention/management of cerebral vasospasm.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
25
Inclusion Criteria
  • aneurysmal subarachnoid hemorrhage
  • potential or actual cerebral vasospasm
Exclusion Criteria
  • non-aneurysmal subarachnoid hemorrhage
  • outside the 4-21 day window after ictus
  • peripheral deoxygenation
  • contraindication for nimodipine administration

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in the cerebral oxygen saturation percentage measured using near infrared spectroscopy technology after administration of nimodipineChange from baseline cerebral oxygen saturation at 30 minutes after administration of nimodipine
Secondary Outcome Measures
NameTimeMethod
Change in the cardiac output measured using near NICOM technology after administration of nimodipineChange from baseline cardiac output at 30 and 240 minutes after administration of nimodipine

unit of measurement will be L/min

Change in the cerebral oxygen saturation percentage measured using near infrared spectroscopy technology after administration of nimodipineChange from baseline cerebral oxygen saturation at 240 minutes after administration of nimodipine

Trial Locations

Locations (1)

NIMHANS

🇮🇳

Bengaluru, India

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