Cerebrovascular DisordersI-IDISNCT02756091
International Intracranial Dissection Study
An observational study of Cerebrovascular Disorders and Vascular: Intracranial, run by Insel Gruppe AG, University Hospital Bern at 3 sites in 2 countries.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Cerebrovascular Disorders, Vascular: Intracranial, Intimal Dissection
- What is being tested?
- No study-specific intervention
- How many people
- 500 participants
- Where
- 3 sitesin 2 countries
- Study dates
- Aug 2016to 30 Nov 2027
- How long will I take part?
- 12 Months
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Patients are recruited in a consecutive ongoing recruitment process in daily clinical practice. Patients who are hospitalized in participant sites are screened by authorized study group members according to local daily practice. If the patient matches the selection criteria (inclusion and exclusion criteria)he/she is enrolled in the study.
Who may be able to join
- Patients with acute Intracranial Artery Dissection (symptom onset ≤ 30 days)
- Age ≥ 18 years
- Consent to participate according to local requirements
Who cannot join
- Iatrogenic dissection caused by endovascular intervention
- Extracranial dissection with intracranial extension
Trial locations and contacts
3 sites in 2 countries. Contact the study team or a site near you to ask about taking part.
Marcel Arnold, Prof. Dr. med. contact
Barbara Goeggel Simonetti, Dr. med. contact
3 sites in 2 countries
Switzerland2 sites, 2 recruiting
- Recruiting
Department of Neurology, University Hospital Basel
Basel, Canton of Basel-City, 4056
Engelter Stefan, Prof. Dr. med.
- Recruiting
Department of Neurology, Inselspital Bern
Bern, 3010
Marcel Arnold, Prof. Dr. med.
Barbara Goeggel-Simonetti, Dr. med.
Japan1 site, 1 recruiting
- Recruiting
National Cerebral and Cardiovascular Center Osaka
Osaka, Kansai, 565-8565
Masatoshi Koga, MD, PHD
About this study
Official title: International Intracranial Artery Dissection Study
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.
Read the detailed description
Cervicocephalic artery dissection corresponds to a hematoma in the wall of a cervical or an intracranial artery and is an important cause of stroke in children and young and middle-aged adults. While extracranial cervical artery dissection (CeAD) has been extensively studied and described, less information is available on pure intracranial artery dissection (IAD) not involving the cervical portion of the artery. Early reports were based exclusively on autopsy series, hence biased towards the most severe cases. The incidence of IAD is unknown, but is probably lower than the incidence of symptomatic CeAD in populations of European origin. The proportion of IAD among all cervicocephalic dissections varies substantially between ethnic and age groups, and depending on study recruitment strategies and ascertainment methods. Indeed, recruitments through departments of neurology are biased towards CeAD and IAD presenting with local symptoms and/or ischaemic stroke while recruitments through departments of neurosurgery or interventional neuroradiology are biased towards IAD presenting with subarachnoid haemorrhage (SAH).Therefore, patients with IAD are managed not only by neurologists, but also by neurosurgeons, and interventional neuroradiologists, each having an incomplete picture of the disease.
The vast majority of reported series of IAD patients come from Asian countries and IAD affects the posterior circulation more frequently than the anterior circulation in these series. This contrasts with CeAD and saccular intracranial aneurysms, which most commonly affect the anterior circulation. 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 SAH IAD than in patients with non-SAH IAD. Furthermore, little information is available on the risk of recurrent IAD as well as risk for recurrent ischaemic and haemorrhagic events. 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 with 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. Patients with SAH IAD are usually treated by surgery or endovascular procedures because up to 40% of the patients experience re-bleeding within the first days after the event. Various surgical and endovascular treatment methods have been proposed for intracranial dissecting aneurysms. When patients are in poor clinical condition or treatment has an unacceptably high complication risk, it can be decided to withhold from surgical or endovascular treatment. In addition, Most non-SAH IAD patients have been treated medically, but the choice of antithrombotic therapy (anticoagulants or antiplatelet agents) has been evaluated neither in randomised trials nor in systematic reviews and meta-analyses of observational data. As a consequence, there is currently no consensus on optimal treatment of IAD.
- Being tested
- No study-specific intervention
- Keywords
- Intracranial Artery Dissection, IAD, Stroke, Observational Study
- Medical subject headings
- Cerebrovascular Disorders, Stroke
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
No study-specific interventionOther
What is being measured
The primary outcome is the main question the study is designed to answer.
Modified Rankin Scale score (mRS score)
The mRS is a standardised valid measure to semi-quantify functional outcome after stroke.
Measured: 180 days after diagnosis +/- 30 days
Recurrence of stroke
Measured: 180 days after diagnosis
Secondary outcomes (7)
Recurrence of cervico- cerebral dissection
Measured: 90 days, 180 days, 12 months
Recurrence of stroke
Measured: 0-10 days, 90 days, 12 months after diagnosis
Change in Modified Rankin Scale score (mRS score) from before diagnosis to follow up
The mRS is a standardised valid measure to semi-quantify functional outcome after stroke.
Measured: 0-10 days, 90 days, 12 months after diagnosis
Change in occupational status from before diagnosis to follow up
The patients' profession, workload (whether the patient is full time or part time working) and, if the patient is not working, the reason why he or she is not working (e.g. for medical reason) are assessed by patient interview according to local routine procedure.
Measured: 0-10 days, 90 days, 180 days, 12 months after diagnosis
Mortality
Measured: 0-10 days, 90 days, 180 days, 12 months after diagnosis
Increase or reduction in size (>50% local degree of stenosis) or disappearance of stenosis at 6 months (in patients with stenotic and occlusive dissection)
Assessed by radiological assessments according to local routine procedures.
Measured: 180 days after diagnosis
Increase or reduction in size (> 20% maximal diameter) of aneurysms at 6 months (in patients with aneurysm)
Assessed by radiological assessments according to local routine procedures.
Measured: 180 days after diagnosis
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 Apr 2016 (estimated)
- Study startAug 2016
- Primary completion30 Nov 2026 (estimated)
- Study completion30 Nov 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cerebrovascular DisordersStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 500 participants (estimated)
- Target duration
- 12 Months
Sponsor and investigators
- Lead sponsor
- Insel Gruppe AG, University Hospital Bern
- Sponsor type
- University, hospital or other
- Collaborators
- Swiss Heart Foundation, Cervical Artery Dissections and Ischemic Stroke Patients - Consortium
- Responsible party
- Sponsor
- Investigators
- Marcel Arnold, Prof. Dr. med., Principal investigator, Neurology Department, Inselspital University Hospital BernBarbara Goeggel Simonetti, Dr. med., Principal investigator, Neurology Department, Inselspital University Hospital Bern
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02756091
- Sponsor's protocol ID
- 2016-00526
- Other IDs
- 2016
- Acronym
- I-IDIS
- Status last verified
- Nov 2024
- First submitted
- 11 Apr 2016
- Last updated
- 13 Nov 2024
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 13 Nov 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- International Intracranial Artery Dissection Study
- ClinicalTrials.gov ID
- NCT02756091
- Acronym / sponsor ID
- I-IDIS / 2016-00526
- Keywords
- Intracranial Artery Dissection, IAD, Stroke, Observational Study
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 500 participants (estimated)
- Lead sponsor
- Insel Gruppe AG, University Hospital BernUniversity, hospital or other
- Collaborators
- Swiss Heart Foundation, Cervical Artery Dissections and Ischemic Stroke Patients - Consortium
- Study start
- Aug 2016
- Primary completion
- 30 Nov 2026 (estimated)
- Study completion
- 30 Nov 2027 (estimated)
- First posted
- 29 Apr 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
Cervicocephalic artery dissection corresponds to a hematoma in the wall of a cervical or an intracranial artery and is an important cause of stroke in children and young and middle-aged adults. While extracranial cervical artery dissection (CeAD) has been extensively studied and described, less information is available on pure intracranial artery dissection (IAD) not involving the cervical portion of the artery. Early reports were based exclusively on autopsy series, hence biased towards the most severe cases. The incidence of IAD is unknown, but is probably lower than the incidence of symptomatic CeAD in populations of European origin. The proportion of IAD among all cervicocephalic dissections varies substantially between ethnic and age groups, and depending on study recruitment strategies and ascertainment methods. Indeed, recruitments through departments of neurology are biased towards CeAD and IAD presenting with local symptoms and/or ischaemic stroke while recruitments through departments of neurosurgery or interventional neuroradiology are biased towards IAD presenting with subarachnoid haemorrhage (SAH).Therefore, patients with IAD are managed not only by neurologists, but also by neurosurgeons, and interventional neuroradiologists, each having an incomplete picture of the disease.
The vast majority of reported series of IAD patients come from Asian countries and IAD affects the posterior circulation more frequently than the anterior circulation in these series. This contrasts with CeAD and saccular intracranial aneurysms, which most commonly affect the anterior circulation. 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 SAH IAD than in patients with non-SAH IAD. Furthermore, little information is available on the risk of recurrent IAD as well as risk for recurrent ischaemic and haemorrhagic events. 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 with 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. Patients with SAH IAD are usually treated by surgery or endovascular procedures because up to 40% of the patients experience re-bleeding within the first days after the event. Various surgical and endovascular treatment methods have been proposed for intracranial dissecting aneurysms. When patients are in poor clinical condition or treatment has an unacceptably high complication risk, it can be decided to withhold from surgical or endovascular treatment. In addition, Most non-SAH IAD patients have been treated medically, but the choice of antithrombotic therapy (anticoagulants or antiplatelet agents) has been evaluated neither in randomised trials nor in systematic reviews and meta-analyses of observational data. As a consequence, there is currently no consensus on optimal treatment of IAD.
Study design
- Observational model
- Other
- Time perspective
- Prospective
- Target follow-up
- 12 Months
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients are recruited in a consecutive ongoing recruitment process in daily clinical practice. Patients who are hospitalized in participant sites are screened by authorized study group members according to local daily practice. If the patient matches the selection criteria (inclusion and exclusion criteria)he/she is enrolled in the study.
Key inclusion criteria (3 listed)
- Patients with acute Intracranial Artery Dissection (symptom onset ≤ 30 days)
- Age ≥ 18 years
- Consent to participate according to local requirements
Key exclusion criteria (2 listed)
- Iatrogenic dissection caused by endovascular intervention
- Extracranial dissection with intracranial extension
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| No study-specific intervention | Other | – |
Primary outcome
Modified Rankin Scale score (mRS score)
Time frame: 180 days after diagnosis +/- 30 days
The mRS is a standardised valid measure to semi-quantify functional outcome after stroke.
Recurrence of stroke
Time frame: 180 days after diagnosis
7 secondary outcomes
Recurrence of cervico- cerebral dissection
Time frame: 90 days, 180 days, 12 months
Recurrence of stroke
Time frame: 0-10 days, 90 days, 12 months after diagnosis
Change in Modified Rankin Scale score (mRS score) from before diagnosis to follow up
Time frame: 0-10 days, 90 days, 12 months after diagnosis
Change in occupational status from before diagnosis to follow up
Time frame: 0-10 days, 90 days, 180 days, 12 months after diagnosis
Mortality
Time frame: 0-10 days, 90 days, 180 days, 12 months after diagnosis
Increase or reduction in size (>50% local degree of stenosis) or disappearance of stenosis at 6 months (in patients with stenotic and occlusive dissection)
Time frame: 180 days after diagnosis
Increase or reduction in size (> 20% maximal diameter) of aneurysms at 6 months (in patients with aneurysm)
Time frame: 180 days after diagnosis
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Nov 2024.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Marcel Arnold, Prof. Dr. med. contact
Barbara Goeggel Simonetti, Dr. med. contact
Marcel Arnold, Prof. Dr. med. principal investigator
Neurology Department, Inselspital University Hospital Bern
Barbara Goeggel Simonetti, Dr. med. principal investigator
Neurology Department, Inselspital University Hospital Bern
3 sites in 2 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Cerebrovascular Disorders and Vascular: Intracranial, run by Insel Gruppe AG, University Hospital Bern at 3 sites in 2 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 13 Nov 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites in Switzerland, Japan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Marcel Arnold, Prof. Dr. med. (marcel.arnold@insel.ch), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Modified Rankin Scale score (mRS score) (time frame: 180 days after diagnosis +/- 30 days). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Nov 2024.