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NCT01934725Active, not recruiting

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

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

Source: ClinicalTrials.gov · Last updated 16 May 2025

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
1200 (estimated)
First submitted
29 Aug 2013
Start date
1 Nov 2013
Primary completion date
31 Dec 2031
Lead sponsor
SECRETO Study Consortium
NCT number
NCT01934725

What you commit to

  • Study type: Observational
  • Planned participants: 1200
  • From 1 Nov 2013 to the primary completion date, 31 Dec 2031
  • 19 sites in 13 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

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

Other illness

  • Other baseline mandatory tests not obtained within the first two weeks following stroke 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 with automated arrhythmia detection for at least 24 hours
    • Screening for thrombophilia, including antiphospholipid antibodies and other coagulopathies (any abnormal finding must be retested at mandatory 3-month follow-up visit \>12 weeks from initial testing or \>4 weeks after cessation of anticoagulation at any later time point); mandatory tests include anticardiolipin antibodies, lupus anticoagulant, anti-β2-glycoprotein antibodies, factor V mutation (or aPC resistency ruled out), factor II mutation, homocysteine, antithrombin III, protein C, and protein S
  • Current stroke due to cerebral venous thrombosis or as a complication of subarachnoid hemorrhage, angiography, or cardiac surgery

Lab values

  • 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

Other

  • No evidence of current brain ischemia
  • Informed consent not obtained from the patient or a proxy.
    • CONTROL SUBJECTS:

Who the study is looking for

  • Age 18 to 49 at stroke onset
  • Patient hospitalized due to first-ever imaging-positive ischemic stroke of undetermined etiology after complete timely diagnostic testing.
  • Age 18 to 49 years
  • Absence of prior ischemic stroke as ascertained using the Questionnaire for Verifying Stroke-Free Status
    • Exclusion Criterion:
    • 1\. Informed consent not obtained

Criteria the registry did not label

  • PATIENTS:

Age in the registry: 18 years to 49 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (19)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ernst-Moritz-Arndt University Medicine
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GreifswaldGermanyUnknown status
Tartu University Hospital
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TartuEstoniaUnknown status
Torrecárdenas University Hospital
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AlmeríaSpainUnknown status
Helsinki University Central Hospital
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HelsinkiFinlandUnknown status
Kuopio University Hospital
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KuopioFinlandUnknown status
Oulu University Hospital
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OuluFinlandUnknown status
Tampere University Hospital
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TampereFinlandUnknown status
Turku University Central Hospital
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TurkuFinlandUnknown status
Peterborough City Hospital
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PeterboroughUnited KingdomUnknown status
Royal Stoke University Hospital
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Stoke-on-TrentUnited KingdomUnknown status
"Attikon" Hospital, University of Athens, School of Medicine
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AthensGreeceUnknown status
University of Brescia
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BresciaItalyUnknown status
Arcispedale S. Maria Nuova
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Reggio EmiliaItalyUnknown status
Vilnius University Hospital Santariškių Klinikos
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VilniusLithuaniaUnknown status
Radboud University Nijmegen Medical Centre
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NijmegenNetherlandsUnknown status
Haukeland University Hospital
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BergenNorwayUnknown status
Hospital Santa Maria
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LisbonPortugalUnknown status
Sahlgrenska University Hospital
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GothenburgSwedenUnknown status
Istanbul University Istanbul Faculty of Medecine
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IstanbulTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.