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Completed

NCT Number: NCT04780022

Patent Foramen Ovale Closure in Older Patients

* Describe the baseline and procedural characteristics of older patients undergoing PFO closure due to cryptogenic embolism. * Assess the long-term follow-up of this cohort, focusing on neurological events and their origin, major cardiac outcomes, as well as survival rates and death origin. * Seek for predictors of neurological event recurrence after the procedure.

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Key information

About this study

In patients with cryptogenic stroke, up to 4 randomized trials and subsequent meta-analyses have recently shown a significant reduction in recurrent ischemic stroke events following percutaneous closure of patent foramen ovale (PFO) . All randomized trials but one excluded patients older than 60 years, and a mean patient age of about 50 years was reported in the single randomized trial including older patients. Thus, whereas PFO closure has been established as the new gold-standard therapy in young patients with cryptogenic stroke and PFO, there are no definite recommendations on the management of patients older than 60 years. Some studies have shown that older patients with cryptogenic stroke exhibit a much higher prevalence of PFO (compared with patients with stroke of known cause), similar to that in younger populations, but scarce data exist on acute and mid-term clinical outcomes of older patients undergoing PFO closure.

The investigators have recently reported the results of study comparing the long-term clinical outcomes of patients older (vs. younger) than 60 years in our centre. A total of 475 consecutive patients (90 older than 60 years) were included, and the main results can be summarized as follows: 1) older patients with cryptogenic embolism and PFO exhibited a higher burden of cardiovascular risk factors; 2) PFO closure was safe in older patients, with no differences in periprocedural complications compared with younger patients; 3) at long-term (median of 8 years) follow-up post-PFO closure, the global mortality rate was higher among older patients, but differences were driven by noncardiovascular mortality (mainly cancer), and 4) the rate of recurrent stroke/TIA was low (much lower than that predicted by the RoPE score), but there was a tendency toward a higher incidence of recurrent stroke/TIA among older patients, which appeared to be partially related to cardiovascular risk factor burden (no differences in recurrent ischemic event rate were observed after adjustment for baseline differences in cardiovascular risk factors between groups). The main limitation of this study was the relatively low number of patients older than 60 years, precluding an appropriate evaluation of the factors associated with poorer clinical outcomes in this population. Thus, the investigators are planning to confirm prior findings in a collaborative project including a much larger cohort of patients. Also, the results of this retrospective study would provide the rationale for a CIHR submission on a randomized trial targeting this group of patients.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients older than 60 years who have experienced a previous paradoxical embolism (stroke, transient ischaemic attack or peripheral embolism) of unknown origin and underwent transcatheter PFO closure.

Exclusion criteria

  • PFO closure indication other than paradoxical embolism (example: platypnea orthodeoxia syndrome).
  • Surgical PFO closure.

Treatment and study plan

Clinical events at last follow-up

Other

Clinical events (stroke, transient ischemic attack, peripheral embolism, deep venous thrombosis, atrial fibrillation, myocardial infarction, bleeding episode, death) at last follow-up

Primary outcomes

  1. Rate of stroke

    Time frame: Through study completion, an average of 1 year

  2. Rate of transient ischemic attack

    Time frame: Through study completion, an average of 1 year

  3. Rate of peripheral embolism

    Time frame: Through study completion, an average of 1 year

  4. Rate of deep venous thrombosis

    Time frame: Through study completion, an average of 1 year

  5. Rate of atrial fibrillation

    Time frame: Through study completion, an average of 1 year

  6. Rate of myocardial infarction

    Time frame: Through study completion, an average of 1 year

  7. Rate of bleeding

    Time frame: Through study completion, an average of 1 year

  8. Rate of death

    Time frame: Through study completion, an average of 1 year

Sponsors and collaborators

Lead sponsor

Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec

Other

Collaborators

  • Hospital Clinic of Barcelona
  • Hospital Clinico de Madrid
  • Montreal Heart Institute
  • Ottawa Heart Institute
  • St. Boniface Hospital
  • Toronto General Hospital

Registry information

Official study title

Patent Foramen Ovale Closure in Older Patients: A Collaborative Multicenter Retrospective Study

Acronym: PFO-Elderly

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Mar 3, 2021
Registry last updated
Mar 2, 2022

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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