Actively Recruiting
Delayed Cerebral Infarction Beyond Endoluminal Spasmolysis and Induced Hypertension
Led by Region Stockholm · Updated on 2025-12-26
200
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
Sponsors
R
Region Stockholm
Lead Sponsor
K
Karolinska Institutet
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are observing patients who have severe cerebral vasospasm following a subarachnoid hemorrhage, either newly developing or already established. This study focuses on monitoring brain blood flow using multiple neuromonitoring methods to better understand delayed cerebral infarction beyond current treatments. The study is sponsored by Region Stockholm and aims to gather detailed data on blood flow velocity after certain interventions. The study involves treatments like induced hypertension using norepinephrine and/or dobutamine to reach target cerebral perfusion pressure, following routine clinical guidelines. Another intervention is endoluminal spasmolysis, which uses intra-arterial Nimodipine to relax cerebral arteries as directed by neurointerventionists. These treatments are evaluated through observational monitoring rather than experimental assignment. Participants will be closely observed in a critical care setting after their subarachnoid hemorrhage. Researchers will measure mean flow velocity in cerebral arteries up to 12 hours after intervention, along with how long changes in flow velocity last after endoluminal spasmolysis. The study collects detailed neuromonitoring data while participants receive standard care, with the total involvement period depending on their clinical course.
CONDITIONS
Brief Title
Delayed Cerebral Infarction Beyond Endoluminal Spasmolysis and Induced Hypertension
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults 18 years or older
- Receiving critical care after subarachnoid haemorrhage
- Aneurysm secured by surgical clipping or endovascular procedure
- Suspected, emerging or established severe cerebral vasospasm
You will not qualify if you...
- Expected survival less than five days as judged by treating clinician
- Transcranial Doppler signal too weak for monitoring
- Pregnancy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 12 hours post intervention
Participants who receive routine care including induced hypertension and endoluminal spasmolysis are observed to assess cerebral perfusion and vasospasm.
Continuous monitoring during clinical care
Trial Site Locations
Total: 1 location
1
Karolinska University Hospital
Stockholm, Sweden, 17176
Actively Recruiting
Research Team
P
Peter C Rudberg, M.D. Ph.D.
A
Anja Rosén, M.D.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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