patent foramen ovale
Conditions
Interventions
percutaneous closure group:None
non percutaneous closure group:None
Sponsors
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.Informed and voluntarily participating in this study, aged >=18 years old; 2.Commit to abide by the research procedures and cooperate with the implementation of the whole process of research; 3.Diagnosed as PFO by TTE/TEE; 4.Generally good health.
Exclusion criteria
Exclusion criteria: 1.Patients with mild or above tricuspid regurgitation (not including mild); 2.Pregnant and lactating women; 3.Patients with hyperlipidemia, hyperglycemia, and hypertension; 4.There is atrial septal defect; 5.There is pulmonary arteriovenous shunt; 6.Atrial fibrillation; 7.Known systemic and pulmonary embolism; 8.Known cardiomyopathy, myocardial infarction, heart valve stenosis and other organic heart diseases.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Abnormal septal morphology;Patent foramen ovale-related hemodynamics;Cardiac hemodynamic changes; | — |
Secondary
| Measure | Time frame |
|---|---|
| Image of cerebral ischemia;Neurological symptoms; | — |
Countries
China
Contacts
Public ContactLiu Manwei
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Outcome results
None listed