Clinical Trials

Toll-Free: 866.320.4573

Call Us Toll Free:

866.223.2273 x1234

Aortic or Mitral Valve Replacement With the Biocor and Biocor Supra


Post-Approval Study Protocol of the St. Jude Medical Biocor and Biocor Supra Valves




The purpose of this study is to further evaluate the long-term safety and effectiveness of the Biocor and Biocor Supra Valves.

Study Status: Active, not recruiting


Condition Intervention Phase
Aortic Valve Insufficiency
Aortic Valve Regurgitation
Aortic Valve Stenosis
Aortic Valve Incompetence
Mitral Valve Insufficiency
Mitral Valve Regurgitation
Mitral Valve Stenosis
Mitral Valve Incompetence
Device: Biocor and Biocor Supra valves N/A

Verified by St. Jude Medical September, 2013

Sponsored by: St. Jude Medical
Information provided by: St. Jude Medical identifier: NCT00636987

Study Type: Interventional

Study Design: Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Cleveland Clinic Foundation
Cleveland, Ohio 44195
United States

Urban Lonn, MD, PhD., Study Director

This information is abridged to display results relevant only to Cleveland Clinic. To see complete record visit
  Information obtained from on
Link to the current record.

Cleveland Clinic Mobile Site