Clinical Trials Logo

Foramen Ovale, Patent clinical trials

View clinical trials related to Foramen Ovale, Patent.

Filter by:

NCT ID: NCT02127294 Completed - Migraine Clinical Trials

Effectiveness and Safety of Transcatheter Patent Foramen Ovale Closure for Migraine

EASTFORM
Start date: January 2013
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate effectiveness and safety of transcatheter patent foramen ovale closure for migraine.

NCT ID: NCT01960491 Completed - Clinical trials for Patent Foramen Ovale (PFO)

FIH Study With CBSO

Start date: May 2014
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the effectiveness and the safety of the intracardiac septal closure device (CBO), as well as the practicability of implantation of this device using the accessories (DS for CBO).

NCT ID: NCT01854281 Completed - Clinical trials for Patent Foramen Ovale

Nitrogen Bubble Detection After Simulated Dives in Divers With PFO and After PFO Closure

Start date: May 2013
Phase: N/A
Study type: Observational

The aim of this study is to determine whether catheter-based closure of patent foramen ovale is effective in preventing paradoxical embolization of nitrogen bubbles after simulated dives.

NCT ID: NCT01780207 Completed - Clinical trials for Obstructive Sleep Apnea

Impact Of Closure Of Patent Foramen Ovale On Apnoea-Hypopnoea-Index, Nocturnal Hypoxemia And Systemic Vascular Function In Patients With Obstructive Sleep Apnoea

Start date: n/a
Phase: N/A
Study type: Interventional

The purpose of this study in patients with obstructive sleep apnoea (OSA) and concomitant patent foramen ovale (PFO) is to assess the impact of percutaneous PFO closure on nocturnal hypoxemia and apnea/hypopnea, pulmonary and systemic artery pressure, endothelial function and arterial stiffness.

NCT ID: NCT01711983 Completed - Clinical trials for Septal Defect, Atrial

Safety and Efficacy of the GORE® Septal Occluder to Treat Ostium Secundum Atrial Septal Defects

Start date: October 2012
Phase: N/A
Study type: Interventional

The primary objective of the GORE® Septal Occluder Study is to evaluate the safety and efficacy of the occluder device in the treatment of transcatheter closure of ostium secundum atrial septal defects (ASDs). The data obtained in this study will evaluate this next generation device as compared to outcomes of prior studies conducted with the GORE® HELEX® Septal Occluder.

NCT ID: NCT01257880 Completed - Migraine With Aura Clinical Trials

Comorbidities Associated With Migraine and Patent Foramen Ovale (CAMP)

CAMP
Start date: January 2010
Phase: N/A
Study type: Observational

The purpose of the study is to compare the rate of comorbidities associated with migraine aura (MA) between persons who have a large circulatory right-to-left shunt (RLS) and those who do not have RLS. Approximately 50% of individuals who have MA also have RLS due to patent foramen ovale (PFO). A PFO is an anatomical opening or flap between the upper chambers of the heart or atria that permits blood to pass from the right of the heart to the left side of the heart, without first going to the lungs to be filtered and oxygenated. Many health conditions and clinical syndromes including stroke, sleep apnea, and migraine have been linked to PFO. Although the mechanism is undetermined, it is hypothesized that microscopic blood clots and chemicals such as serotonin can pass through the PFO, travel to the brain, and cause headache and aura. Persons who have MA are at increased risk for stroke and transient ischemic attacks relative to people who do not have migraine. Migraine is also associated with the presence of white matter lesions in the brain and mild deficits in cognitive function associated with the posterior brain (vision, memory, processing speed). The risk of stroke in migraine is highest for women under the age of 45 who have aura and a high number of migraine headache days per month. No convincing evidence has been produced to explain the mechanism for the increased risk of ischemic stroke in migraine; however, increased platelet activation and aggregation is a plausible theory. We hypothesize that migraineurs with aura and large RLS (presumably due to a PFO) will be more likely to have sleep apnea, increased platelet activation, cognitive deficits, alterations in cerebral vasomotor function, and white matter lesions than migraineurs with aura who do not have PFO. The results of this exploratory study will generate hypotheses as to why subgroups of migraineurs have an increased risk of stroke and the impact of large PFO on comorbid conditions associated with migraine aura. Early identification of migraine subgroups with a constellation of clinical syndromes that increase risk of neurovascular diseases will allow initiation of preventive strategies that may ultimately reduce burden and improve the productive quality of life for these individuals.

NCT ID: NCT01216423 Completed - Pulmonary Embolism Clinical Trials

Pulmonary Embolism and Stroke in Patient With Patent Foramen Ovale

EPIC-FOP
Start date: November 2009
Phase: N/A
Study type: Observational

The cause of ischemic stroke remains frequently unknown. In patients with patent foramen ovale (PFO), the link between PFO and Stroke is unclear. The investigators hypothesize that the main mechanism is paradoxical embolism and decided to look for clinically apparent and silent cerebral embolism in patients with a recent pulmonary embolism.

NCT ID: NCT00968032 Completed - Clinical trials for Foramen Ovale, Patent

Procedural Success and Safety of the Nit-Occlud® Patent Foramen Ovale (PFO) Closure Device and Its Application System

09k003
Start date: July 2009
Phase: N/A
Study type: Interventional

The foramen ovale is an opening in the interatrial septum. It results from an incomplete coverage of the ostium secundum. In 10 to 24% of the general population incomplete fibrosis of the interatrial septum is a clinical finding and is defined as a patent foramen ovale (PFO). The Nit-Occlud® PFO umbrella is a permanent implant for closing PFOs that is implanted in the PFO using minimally invasive catheter technology. The umbrella is made from Nitinol, a material with superelastic properties, which, in its relaxed state, has the form of a double umbrella. This is a single-center, non-comparative, prospective interventional clinical investigation involving 1 center in Germany to assess the effectiveness, safety and practicability of implantation of the Nit-Occlud PFO® Closure Device.

NCT ID: NCT00831259 Completed - Pulmonary Embolism Clinical Trials

Risk of Stroke in Pulmonary Embolism With a Patent Foramen Ovale (PFO)

ICEP
Start date: October 2007
Phase: N/A
Study type: Observational

Pulmonary embolism is associated with a small but definite risk of paradoxical embolism in patients with a patent foramen ovale (PFO). While neurologic complications are unfrequent the incidence of clinically silent brain infarction is unknown. We will assess the rate of clinically apparent and silent cerebral embolism in patients with a pulmonary embolism (PE) in relation to the presence or not of a PFO.

NCT ID: NCT00750594 Completed - Migraine Headaches Clinical Trials

Patent Foramen Ovale in Children With Migraine Headaches

Start date: April 2008
Phase: N/A
Study type: Observational

This study will be the first to provide data about the relationship between PFO and migraine in children. By establishing the actual prevalence, we will better understand if PFO plays a role in the occurence of pediatric migraine and, thus, provide the incentive to perform additional studies evaluating whether PFO closure is an effective treatment option for pediatric migraine. For children with migraine headaches, discovering novel and effective treatments would be life altering.