Foramen Ovale, Patent Clinical Trial
Official title:
Suture Mediated Septal Defect Closure/Repair Evaluation of the NobleStitch EL System
The purpose of the STITCH study is to evaluate closure rates of clinically relevant septal defects, including patent foramen ovale (PFO), Atrial Septal Defects (ASD - less than 1 cm with redundant septal tissue), trans septal puncture sites, repair of Atrial Septal Aneurysm (ASA) and rate of recurrent neurologic embolic events in patients with cryptogenic stroke and PFO.
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Status | Clinical Trial | Phase | |
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Completed |
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Recruiting |
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Completed |
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Patent Foramen Ovale and the Risk of Postoperative Delirium Following Elective Hip and Knee Arthroplasty Surgeries
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N/A | |
Recruiting |
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Completed |
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Completed |
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N/A | |
Recruiting |
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Long-term Outcomes After Percutaneous Closure of PFO
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Completed |
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Effectiveness and Safety of Transcatheter Patent Foramen Ovale Closure for Migraine
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N/A | |
Recruiting |
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Prospective Clinical Follow-up After the Percutaneous Closure of a Patent Foramen Ovale
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N/A | |
Enrolling by invitation |
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Stitch Closure of PFO and Septal Repair (STITCH)
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N/A | |
Suspended |
NCT04339699 -
NobleStitch EL STITCH Trial is a PFO Comparative Trial
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N/A | |
Recruiting |
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Investigation of Nickel Sensitization After Percutaneous Implantation of Patent Foramen Ovale Occluder
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N/A | |
Withdrawn |
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Patent Foramen Ovale (PFO) Closure at the Time of Endovascular Cardiac Electronic Device Implantation
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N/A |