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Clinical Trials in Japan / NCT02756091
Recruiting Observational

International Intracranial Dissection Study

NCT02756091 · tracked via the Priya Life Science Japan tracker
Phase
Observational
Started
2016-08
Last updated
2024-11-13

Condition(s) studied

Cerebrovascular DisordersVascular: IntracranialIntimal DissectionStroke

Investigational drug(s) / intervention(s)

No study-specific intervention

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients with acute Intracranial Artery Dissection (symptom onset ≤ 30 days) * Age ≥ 18 years * Consent to participate according to local requirements Exclusion Criteria: * Iatrogenic dissection caused by endovascular intervention * Extracranial dissection with intracranial extension

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
National Cerebral and Cardiovascular Center Osaka Osaka Kansai Recruiting
Department of Neurology, University Hospital Basel Basel Canton of Basel-City Recruiting
Department of Neurology, Inselspital Bern Bern Switzerland Recruiting

More Insel Gruppe AG, University Hospital Bern trials in Japan

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT02756091 on ClinicalTrials.gov ↗ ← All trials in Japan