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Life sciences · Interventional Study
ClinicalTrials.gov · October 2, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Interventional Study.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
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Registry record from ClinicalTrials.gov (NCT03523416). This is a study registration, not published results. Lead sponsor: Edwards Lifesciences. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 90 participants (ESTIMATED). Conditions: Heart Failure. Interventions: DEVICE: Edwards APTURE transcatheter shunt system. Primary outcome measures: Rate of major cardiac/cerebrovascular/renal events and re-intervention (Safety Endpoint) , 30 days. Brief summary: The purpose of this study is to evaluate initial clinical safety, device functionality and effectiveness of the Edwards APTURE transcatheter shunt system.