Actively Recruiting

Age: 18Years +
All Genders
ID07305922

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

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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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

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

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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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