Efficacy and Safety of Percutaneous Foramen Ovale Closure in Adult Patients with Drug-resistant Epilepsy and Patent Foramen Ovale: a Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Patent foramen ovale (PFO) is the most common cause of right-to-left shunt (RLS) in the adult heart, with a prevalence of approximately 25% in the general population. Extensive research has demonstrated an association between PFO and neurological conditions such as cryptogenic stroke, migraine, and sleep apnea syndrome, and it is even considered a potential root cause of these disorders. However, the mechanisms by which PFO contributes to neurological diseases remain unclear. In our preliminary clinical work, we have observed a strong correlation between PFO and epilepsy, and PFO closure has shown some efficacy in reducing seizure frequency. The aim of this study is to further investigate the efficacy and safety of PFO closure in patients with drug-resistant epilepsy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 60
Healthy Volunteers: f
View:

• Age between 18 and 60 years, with no gender restrictions;

• Diagnosis of epilepsy in accordance with the International League Against Epilepsy (ILAE) criteria (2014 edition);

• Drug-resistant epilepsy, defined as failure to achieve sustained seizure freedom despite appropriate selection and tolerability of at least two antiseizure medications (monotherapy or combination therapy) for a minimum of six months;

• Diagnosis of patent foramen ovale (PFO) meeting the criteria established by the American Society of Echocardiography (ASE) and the Society for Cardiovascular Angiography and Interventions (SCAI) (2015 edition), with right-to-left shunting (RLS) of grade II or higher upon Valsalva maneuver, as assessed by contrast-enhanced echocardiography;

• Stable antiseizure medication regimen for at least four weeks prior to screening, with willingness to maintain a stable regimen throughout the study period;

• At least one documented seizure episode during a six-week screening period (with a minimum of four weeks of effective seizure diary recordings) and a retrospective self-reported history of at least 12 seizures in the year preceding screening;

• Ability to independently or with caregiver assistance complete a seizure diary and comply with clinical data collection and required medical examinations;

• Willingness to undergo the investigational treatment and voluntary provision of written informed consent.

Locations
Other Locations
China
Westchina Hospital
RECRUITING
Chengdu
Contact Information
Primary
Lei Chen
leilei_25@126.com
+8618980605819
Time Frame
Start Date: 2025-02-28
Estimated Completion Date: 2027-06-01
Participants
Target number of participants: 180
Treatments
Experimental: Operation group
patent foramen ovale closure
No_intervention: control group
Sponsors
Leads: Sichuan University

This content was sourced from clinicaltrials.gov