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NCT Number: NCT04475510

Discontinuation of Antithrombotic Treatment Following Patent Foramen Ovale Closure in Young Patients With Cryptogenic Stroke

To determine the safety of antithrombotic treatment discontinuation 12 months following successful transcatheter PFO closure.

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Key information

About this study

Young patients with a cryptogenic ischemic event undergoing transcatheter PFO closure exhibit a low but clinically relevant risk of bleeding (overall and major bleeding) at long-term follow-up, eventually exceeding the risk of ischemic events.

Importantly, the vast majority of major bleeding events seem to occur in patients receiving antiplatelet therapy. Preliminary data suggest that antiplatelet therapy discontinuation is not associated with any increase in ischemic events, and could potentially translate into a lower rate of major bleeding events at longer term follow-up. We therefore hypothesize that in young patients without any other comorbidities increasing the risk of stroke, shorter-term (≤1 year instead of lifelong) antiplatelet treatment could be a safe option following PFO closure.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Successful transcatheter PFO closure with any approved device
  • Patients ≤60 years diagnosed with a cryptogenic stroke/TIA who have undergone successful transcatheter PFO closure

Exclusion criteria

->60 year-old

  • RoPE score <6
  • Residual shunt ≥moderate following PFO closure
  • Atrial fibrillation following PFO closure
  • Presence of ≥2 cardiovascular risk factors (smoking, hypertension, dyslipidemia)
  • Diabetes mellitus
  • Thrombophilia (factor V Leiden, factor II mutation, anticardiolipin antibodies, lupus anticoagulant, anti-b2 glycoprotein-I antibodies, protein C deficiency, protein S deficiency)
  • Recurrent cerebrovascular event (stroke, TIA) within the year following PFO closure
  • Failure to provide signed informed consent
  • Absolute contraindications for an MRI study

Treatment and study plan

Antiplatelet treatment discontinuation

Other

All patients will undergo a clinical evaluation and cerebral MRI at 12 months (before antiplatelet treatment cessation) and at 24 months post-PFO closure.

Primary outcomes

  1. Presence of new stroke events

    Time frame: 12 months

    1)Acute episode of a focal or global neurological deficit with at least one of the following: change in level of consciousness, hemiplegia, hemiparesis, numbness or sensory loss affecting one side of the body, dysphasia or aphasia, hemianopia, amaurosis fugax or other new neurological symptom(s) consistent with stroke.(2)Duration of a focal or global neurological deficit ≥ 24 hours OR < 24 hours if available neuroimaging documents a new hemorrhage or infarct; OR the neurological deficit results in death.

  2. Presence of new ischemic lesions

    Time frame: 24-month follow-up

    Evaluated by MRI

Secondary outcomes

  1. Number of new cerebral ischemic lesions

    Time frame: 24-month follow-up

    Evaluated by MRI

  2. Volume of new cerebral ischemic lesions

    Time frame: 24-month follow-up

    Evaluated by MRI

  3. Number of ischemic events

    Time frame: 24-month follow-up

    Stroke, TIA

  4. Number of ischemic events

    Time frame: 3-year follow-up

    Stroke, TIA

  5. Number of ischemic events

    Time frame: 4-year follow-up

    Stroke, TIA

  6. Number of ischemic events

    Time frame: 5-year follow-up

    Stroke, TIA

  7. Number of ischemic events

    Time frame: 6-year follow-up

    Stroke, TIA

  8. Number of ischemic events

    Time frame: 7-year follow-up

    Stroke, TIA

  9. Number of ischemic events

    Time frame: 8-year follow-up

    Stroke, TIA

  10. Number of ischemic events

    Time frame: 9-year follow-up

    Stroke, TIA

  11. Number of ischemic events

    Time frame: 10-year follow-up

    Stroke, TIA

  12. Rate of bleeding

    Time frame: 24-month follow-up

    Life-threatening, major or minor bleeding

  13. Rate of bleeding

    Time frame: 3-year follow-up

    Life-threatening, major or minor bleeding

  14. Rate of bleeding

    Time frame: 4-year follow-up

    Life-threatening, major or minor bleeding

  15. Rate of bleeding

    Time frame: 5-year follow-up

    Life-threatening, major or minor bleeding

  16. Rate of bleeding

    Time frame: 6-year follow-up

    Life-threatening, major or minor bleeding

  17. Rate of bleeding

    Time frame: 7-year follow-up

    Life-threatening, major or minor bleeding

  18. Rate of bleeding

    Time frame: 8-year follow-up

    Life-threatening, major or minor bleeding

  19. Rate of bleeding

    Time frame: 9-year follow-up

    Life-threatening, major or minor bleeding

  20. Rate of bleeding

    Time frame: 10-year follow-up

    Life-threatening, major or minor bleeding

Study contacts

Contact information is provided by the study sponsor or research team.

Josep Rodes-Cabau, MD

CONTACT

[email protected]

4186568711

Melanie Cote, MSc

CONTACT

[email protected]

14186537270

Sponsors and collaborators

Lead sponsor

Josep Rodes-Cabau

Other

Registry information

Official study title

Discontinuation of Antithrombotic Treatment Following Patent Foramen Ovale Closure in Young Patients With Cryptogenic Stroke. The HALTI Trial

Acronym: HALTI

Important dates

Study start
2020
Primary completion
2026
Study completion
2032
First posted
Jul 17, 2020
Registry last updated
Mar 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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