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Establishment of a multidimensional prognostic model for cerebral artery dissection based on gene and imaging analysis

Establishment of a multidimensional prognostic model for cerebral artery dissection based on gene and imaging analysis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000037129
Enrollment
Unknown
Registered
2020-08-27
Start date
2020-12-01
Completion date
Unknown
Last updated
2020-10-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral artery dissection

Interventions

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Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Symptomatic (ischemic stroke or TIA occurring within 2 weeks) patients with intracranial and extracranial arterial or non-stroke patients with asymptomatic; 2. Patients with intracranial and extracranial large (including internal carotid, vertebral, basilar, middle cerebral, etc.), with image support for or probable: (1) Head and neck CTA, TOF MRA/CE MRA or DSA may highly suggest the possibility of arterial if the following signs are present: 1) Beaded or wavy stenosis of blood vessels; 2) Smooth or irregular thinning of blood vessels (typical manifestations are"rat tail sign"and"linear sign"); 3) Obvious vascular intimal flap (valve sign); 4) The blood vessels gradually become thinner to occlusion (typically manifested as"flame sign"); 5) There is double-lumen phenomenon in blood vessels (double-lumen sign); 6) There are double lumens in the blood vessels accompanied by significant rumen dilatation (dissecting aneurysm); (2) HR-MRI evidence of intravascular hematoma and/or intimal flap, except bleeding from atherosclerotic plaques (conditional centers); 3. Agree to obtain blood sample; 4. Voluntarily sign the subject's informed consent form.

Exclusion criteria

Exclusion criteria: 1. Unable to complete imaging (CT or MRI) assessment; 2. Pregnant women; 3. Patients with malignant tumors and other diseases due to the presence of the expected survival of less than 6 months; 4. Patients are receiving experimental drugs and experimental instrument treatment; 5. The doctor believes that it is not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Vascular imaging changes: degree of lumen recanalization, intraluminal thrombus, changes in vessel wall signal, etc.;gene expression profiling;SEN, SPE, ACC, AUC of ROC, PPV, NPV;

Secondary

MeasureTime frame
Stroke Recurrence;All-cause mortality;Post-stroke disability;Life-threatening bleeding;

Countries

China

Contacts

Public ContactXiang Han

Department of Neurology, Huashan Hospital, Fudan University

hansletter@163.com+86 13512115517

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026