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Clinical trial

Impact of Postdilatation With the InterValve V8 Aortic Valvuloplasty Balloon Following Medtronic CoreValve or Other Self-Expanding TAVI Procedure (PostCorE)

NCT02472106 is registered in ClinicalTrials.gov with InterValve, Inc. as lead sponsor.

NCT NCT02472106
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Registry record

As filed in ClinicalTrials.gov.

Title
Impact of Postdilatation With the InterValve V8 Aortic Valvuloplasty Balloon Following Medtronic CoreValve or Other Self-Expanding TAVI Procedure (PostCorE)
Lead sponsor
InterValve, Inc.
Phase
Observational
Overall status
Completed
Start date
June 30, 2015
Completion date
August 31, 2016
Enrollment
9 (actual)
Sites
Not reported

Conditions

As the registry lists them; a condition with its own page is linked.

aortic valve stenosis