Actively Recruiting
Detection of an Endovascular Treatment Target in Patients With an Acute, Spontaneous Intracerebral Hemorrhage
Led by University Hospital, Basel, Switzerland · Updated on 2025-04-11
15
Participants Needed
1
Research Sites
214 weeks
Total Duration
On this page
Sponsors
U
University Hospital, Basel, Switzerland
Lead Sponsor
C
Clinical Trial Unit, University Hospital Basel, Switzerland
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study is to determine if a treatment target for a potential endovascular therapy exists in patients with an acute, spontaneous (non-traumatic) ICH.
CONDITIONS
Official Title
Detection of an Endovascular Treatment Target in Patients With an Acute, Spontaneous Intracerebral Hemorrhage
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of an acute spontaneous intracerebral hemorrhage based on non-contrast CT
- Time from symptom onset to anticipated start of cerebral DSA under 3 hours
- Agreement of the treating physician to perform DSA
- Informed consent by signature or emergency consent procedures
You will not qualify if you...
- High probability that bleeding is caused by ruptured aneurysm, arteriovenous malformation, or amyloid angiopathy as judged by physician
- Planned time-critical surgical or minimally invasive intervention
- Evidence of ongoing pregnancy; negative pregnancy test required for persons of childbearing potential
- Contraindications to iodine contrast media
- Known severe kidney insufficiency (glomerular filtration rate < 30 ml/min)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Department of Neuroradiology, University Hospital Basel
Basel, Switzerland, 4031
Actively Recruiting
Research Team
A
Alex Brehm, PhD
CONTACT
M
Marios-Nikos Psychogios, Prof Dr
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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