Genetic, Metabolic, and Growth Factor Repository for Cerebrovascular Disorders

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCedars-Sinai Medical Center

About this trial

This study encompasses the maintenance and utilization of a repository of samples from patients with cerebrovascular disease and stroke. The types of tissue taken are blood, cerebrospinal fluid (CSF), tissue, and microdialysis samples. Future analysis of these samples can potentially help investigators to better categorize groups of patients, understand the underlying etiology of these pathologies, identify markers that are associated with favorable or poor outcomes, and track changes that occur during the natural course of the disease or with treatment. This is a prospective observational study which will use samples from such patients to create this library which can be used to explore these questions in the future.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

All patients diagnosed with cerebral vascular disease, regardless of gender, age, ethnicity/race, stage of disease or treatment, are eligible.

Expected availability of clinical follow up data

Participants must be willing to provide written, informed consent obtained in accordance with institutional and federal guidelines.

Disqualifiers

Pregnant women are excluded from the study.

Trial population

All patients diagnosed with cerebrovascular disease. This includes both non-surgical patients (such medically managed ischemic stroke, aneurysms, moyamoya disease, arteriovenous malformation, hemorrhagic stroke, etc.) and surgically treated patients (patients with aneurysm coiling or clipping, arteriovenous malformation resection, direct or indirect revascularization procedures for ischemia, etc.).

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

900 Participants
are grouped into 1 trial group
Group A: Repository Group

Trial outcomes

Primary outcomes

1

Change in modified Rankin Scale (mRS) score

Time frame
Baseline, 1 Month, 3 Months, and 6 Months
2

Change in NIH Stroke Scale score

Time frame
Baseline, 1 Month, 3 Months, and 6 Months
3

Change in Barthel Index

Time frame
Baseline, 1 Month, 3 Months, and 6 Months
4

Change in Montreal Cognitive Assessment test score

Time frame
Baseline, 1 Month, 3 Months, and 6 Months

Secondary outcomes

1

Change in Angiographic Neovascularization

Analyzed in digital subtraction angiography (DSA) images

Time frame
Baseline and 6 Months
2

Change in Angiogenic Factor Measurements

Measured in blood, CSF, microdialysis samples, and tissue

Time frame
Baseline, 1 Month, 3 Months, 6 Months

Other outcomes

Sponsors and contacts

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