Actively Recruiting

Age: 18Years +
All Genders
NCT02756091

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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

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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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