IUCPQ
Québec, Quebec, G1V 4G5, Canada
Location status: Recruiting
Location contact
Josep Rodes-Cabau, MD
CONTACT
Josep Rodes-Cabau, MD
PRINCIPAL_INVESTIGATOR
Melanie Cote, MSc
CONTACT
4186568711 ext. Rodes-Cabau
NCT Number: NCT04475510
To determine the safety of antithrombotic treatment discontinuation 12 months following successful transcatheter PFO closure.
Interested in participating?
Request Info18 year–60 year
All sexes
Interventional
Not applicable
Québec, Quebec, G1V 4G5, Canada
Location status: Recruiting
Josep Rodes-Cabau, MD
CONTACT
Josep Rodes-Cabau, MD
PRINCIPAL_INVESTIGATOR
Melanie Cote, MSc
CONTACT
4186568711 ext. Rodes-Cabau
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
->60 year-old
All patients will undergo a clinical evaluation and cerebral MRI at 12 months (before antiplatelet treatment cessation) and at 24 months post-PFO closure.
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.
Time frame: 24-month follow-up
Evaluated by MRI
Time frame: 24-month follow-up
Evaluated by MRI
Time frame: 24-month follow-up
Evaluated by MRI
Time frame: 24-month follow-up
Stroke, TIA
Time frame: 3-year follow-up
Stroke, TIA
Time frame: 4-year follow-up
Stroke, TIA
Time frame: 5-year follow-up
Stroke, TIA
Time frame: 6-year follow-up
Stroke, TIA
Time frame: 7-year follow-up
Stroke, TIA
Time frame: 8-year follow-up
Stroke, TIA
Time frame: 9-year follow-up
Stroke, TIA
Time frame: 10-year follow-up
Stroke, TIA
Time frame: 24-month follow-up
Life-threatening, major or minor bleeding
Time frame: 3-year follow-up
Life-threatening, major or minor bleeding
Time frame: 4-year follow-up
Life-threatening, major or minor bleeding
Time frame: 5-year follow-up
Life-threatening, major or minor bleeding
Time frame: 6-year follow-up
Life-threatening, major or minor bleeding
Time frame: 7-year follow-up
Life-threatening, major or minor bleeding
Time frame: 8-year follow-up
Life-threatening, major or minor bleeding
Time frame: 9-year follow-up
Life-threatening, major or minor bleeding
Time frame: 10-year follow-up
Life-threatening, major or minor bleeding
Contact information is provided by the study sponsor or research team.
Josep Rodes-Cabau, MD
CONTACT
Melanie Cote, MSc
CONTACT
Josep Rodes-Cabau
Other
Discontinuation of Antithrombotic Treatment Following Patent Foramen Ovale Closure in Young Patients With Cryptogenic Stroke. The HALTI Trial
Acronym: HALTI
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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