Searching for Explanations for Cryptogenic Stroke in the Young: Revealing the Etiology, Triggers, and Outcome

Last updated: May 13, 2025
Sponsor: SECRETO Study Consortium
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

Stroke

Cerebral Ischemia

Thrombosis

Treatment

N/A

Clinical Study ID

NCT01934725
SECRETO
  • Ages 18-49
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

BACKGROUND: In industrialized countries a considerable and increasing proportion of strokes occur at younger ages. Stroke at young age causes marked disability at worst and thus long-standing socioeconomic consequences and exposes survivors for 4-fold risk of premature death compared with background population. Up to 50% of young patients with ischemic stroke remain without definitive etiology for their disease despite extensive modern diagnostic work-up (i.e. cryptogenic stroke). The group of cryptogenic strokes includes those with patent foramen ovale (PFO) or other abnormalities in the atrial septum in the heart as the only or concomitant finding. Population prevalence of PFO is high, 25%, and the mechanisms how PFO would be associated causally with ischemic stroke remain to be clarified. Moreover, there are only scarce data on clinical outcome, long-term risk of new vascular events, and prevention of such events in these patients.

DESIGN: Searching for Explanations for Cryptogenic Stroke in the Young: Revealing the Etiology, Triggers, and Outcome (SECRETO) is an international prospective multicenter case-control study of young adults (age 18-49) presenting with an imaging-positive first-ever ischemic stroke of undetermined etiology (aim N=2000). Patients are included after standardized diagnostic procedures (brain MRI, imaging of intracranial and extracranial vessels, cardiac imaging, and screening for coagulopathies) and age- and sex-matched to healthy controls in a 1:1 fashion. Up to 45 study sites worldwide will be needed to recruit the planned participant population during a 3-year period. Neurovascular imaging and echocardiography studies, and ECGs will be read centrally.

AIMS: SECRETO involves five principal fields of investigation: (1) Stroke triggers and clinical risk factors; (2) Long-term prognosis (new vascular events, functional and psychosocial outcomes); (3) Abnormalities of thrombosis and hemostasis; (4) Biomarkers of e.g. inflammation, atherogenesis, endothelial function, thrombosis, platelet activation, and hemodynamic stress to characterize postulated cryptogenic stroke mechanisms; and (5) genetic study, including genome-wide association and candidate gene studies as well as next-generation sequencing approach. All analyses consider cardiac functional and interatrial structural properties as a possible mediator. Furthermore, SECRETO Family Study (substudy) aims at collecting extensive family history of thrombotic events from informative patients being screened for SECRETO main study and collect genetic samples from all consenting family members for whole-genome sequencing.

SIGNIFICANCE: SECRETO will provide novel information on clinical and subclinical risk factors, both transient and chronic, predisposing to cryptogenic ischemic stroke in young adults. This study also reveals long-term prognosis of this understudied patient population and may discover new genetic background underlying the disease mechanism and provide potential targets for drug development.

Eligibility Criteria

Inclusion

PATIENTS:

Inclusion Criteria:

  1. Age 18 to 49 at stroke onset

  2. Patient hospitalized due to first-ever imaging-positive ischemic stroke ofundetermined etiology after complete timely diagnostic testing.

Exclusion

Exclusion Criteria:

  1. Baseline mandatory tests not obtained in the first week following stroke onset,including:
  • Brain MRI

  • Routine blood tests, including complete blood count, CRP, fasting glucose,creatinine, aPTT, INR, total cholesterol, LDL-cholesterol, HDL-cholesterol,HbA1C, hemoglobin electrophoresis in individuals of African origin

  1. Other baseline mandatory tests not obtained within the first two weeks followingstroke onset, including:
  • Imaging of cervicocephalic arteries by CTA, MRA, or DSA

  • Transesophageal (highly recommended) or transthoracic echocardiography

  • 24-hour Holter monitoring or continuous in-hospital ECG monitoring withautomated arrhythmia detection for at least 24 hours

  • Screening for thrombophilia, including antiphospholipid antibodies and othercoagulopathies (any abnormal finding must be retested at mandatory 3-monthfollow-up visit >12 weeks from initial testing or >4 weeks after cessation ofanticoagulation at any later time point); mandatory tests includeanticardiolipin antibodies, lupus anticoagulant, anti-β2-glycoproteinantibodies, factor V mutation (or aPC resistency ruled out), factor IImutation, homocysteine, antithrombin III, protein C, and protein S

  1. No evidence of current brain ischemia

  2. Current stroke due to cerebral venous thrombosis or as a complication ofsubarachnoid hemorrhage, angiography, or cardiac surgery

  3. Patient otherwise not eligible for the study or adherent for follow-up (egnonresident) or has concurrent disease affecting outcome (eg multiple sclerosis,cancer)

  4. Informed consent not obtained from the patient or a proxy.

CONTROL SUBJECTS:

Inclusion Criteria:

  1. Age 18 to 49 years

  2. Absence of prior ischemic stroke as ascertained using the Questionnaire forVerifying Stroke-Free Status

Exclusion Criterion:

  1. Informed consent not obtained

Study Design

Total Participants: 1200
Study Start date:
November 01, 2013
Estimated Completion Date:
December 31, 2031

Connect with a study center

  • Medical University Graz

    Graz, 8036
    Austria

    Site Not Available

  • University Hospitals Leuven

    Leuven, 3000
    Belgium

    Site Not Available

  • CHUM - Hôpital Notre-Dame

    Montreal, Quebec H2L 4M1
    Canada

    Site Not Available

  • Tartu University Hospital

    Tartu,
    Estonia

    Site Not Available

  • Helsinki University Central Hospital

    Helsinki, FI-00029
    Finland

    Site Not Available

  • Kuopio University Hospital

    Kuopio, 70029
    Finland

    Site Not Available

  • Oulu University Hospital

    Oulu,
    Finland

    Site Not Available

  • Tampere University Hospital

    Tampere,
    Finland

    Site Not Available

  • Turku University Central Hospital

    Turku,
    Finland

    Site Not Available

  • Hôpital Roger Salengro

    Lille, F-59037
    France

    Site Not Available

  • Hôpital Sainte-Anne

    Paris, 75014
    France

    Site Not Available

  • Hôpital de Rangueil

    Toulouse, 31403
    France

    Site Not Available

  • University Hospital Giessen

    Giessen, 35392
    Germany

    Site Not Available

  • Ernst-Moritz-Arndt University Medicine

    Greifswald,
    Germany

    Site Not Available

  • Klinikum der Stadt Ludwigshafen a. Rh.

    Ludwigshafen, 67063
    Germany

    Site Not Available

  • "Attikon" Hospital, University of Athens, School of Medicine

    Athens,
    Greece

    Site Not Available

  • University of Brescia

    Brescia, 25123
    Italy

    Site Not Available

  • Arcispedale S. Maria Nuova

    Reggio Emilia,
    Italy

    Site Not Available

  • Vilnius University Hospital Santariskiu klinikos

    Vilnius,
    Lithuania

    Site Not Available

  • Radboud University Nijmegen Medical Centre

    Nijmegen, 6500 HB
    Netherlands

    Site Not Available

  • Haukeland University Hospital

    Bergen, 5021
    Norway

    Site Not Available

  • Hospital Santa Maria

    Lisboa, 1649-035
    Portugal

    Site Not Available

  • Torrecárdenas University Hospital

    Almería,
    Spain

    Site Not Available

  • La Paz University Hospital

    Madrid, 28046
    Spain

    Site Not Available

  • Sahlgrenska University Hospital

    Gothenburg,
    Sweden

    Site Not Available

  • University Hospital Basel

    Basel, CH-4031
    Switzerland

    Site Not Available

  • Istanbul University Istanbul Faculty of Medecine

    Istanbul,
    Turkey

    Site Not Available

  • Peterborough City Hospital

    Peterborough,
    United Kingdom

    Site Not Available

  • Royal Stoke University Hospital

    Stoke-on-Trent,
    United Kingdom

    Site Not Available

  • St. Jude Medical Center

    Fullerton, California 92835
    United States

    Site Not Available

  • Massachusetts General Hospital

    Boston, Massachusetts 02116
    United States

    Site Not Available

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