Actively Recruiting
International Intracranial Dissection Study
Led by Insel Gruppe AG, University Hospital Bern · Updated on 2024-11-13
500
Participants Needed
3
Research Sites
591 weeks
Total Duration
On this page
Sponsors
I
Insel Gruppe AG, University Hospital Bern
Lead Sponsor
S
Swiss Heart Foundation
Collaborating Sponsor
AI-Summary
What this Trial Is About
Cervicocerebral artery dissection is a major cause for stroke in young adults. While knowledge of cervical artery dissection (CeAD) has increased thanks to a number of high quality studies, knowledge on intracranial artery dissection (IAD) is limited. Due to treatment and publication bias little is known about the natural history of IAD. Overall, IAD is assumed to have a more severe course than CeAD, with a more ominous outcome in patients with subarachnoid hemorrhage (SAH). Furthermore, little information is available on the risk of recurrent IAD as well as on the risk of recurrent ischemic and haemorrhagic events in non-Asian patients. Radiological diagnosis of IAD can be challenging given the small size of intracranial arteries, and the subtle and non-specific radiological signs which tend to evolve over time. The optimal treatment of IAD is unknown. There are no randomised trials and only observational studies with relatively small sample sizes are available, thus providing a very low level of evidence. Finding the factors that are decisive for outcome and recurrence after intracranial artery dissection is key to an improved management of this potentially severe disease predominantly affecting young patients. By using standardised protocols for diagnosis, imaging and follow-up, the investigators intend to obtain large representative patient samples in order to fill the gap of evidence.
CONDITIONS
Official Title
International Intracranial Dissection Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with acute Intracranial Artery Dissection (symptom onset 64 30 days)
- Age 65 years
- Consent to participate according to local requirements
You will not qualify if you...
- Iatrogenic dissection caused by endovascular intervention
- Extracranial dissection with intracranial extension
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
National Cerebral and Cardiovascular Center Osaka
Osaka, Kansai, Japan, 565-8565
Actively Recruiting
2
Department of Neurology, University Hospital Basel
Basel, Canton of Basel-City, Switzerland, 4056
Actively Recruiting
3
Department of Neurology, Inselspital Bern
Bern, Switzerland, 3010
Actively Recruiting
Research Team
M
Marcel Arnold, Prof. Dr. med.
CONTACT
B
Barbara Goeggel Simonetti, Dr. med.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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