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Sponsored by: |
Boston Scientific Corporation |
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Information provided by: | Boston Scientific Corporation |
ClinicalTrials.gov Identifier: | NCT00604903 |
This study will evaluate an implantable pulmonary artery pressure sensor in patients with heart failure.
Condition | Intervention |
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Heart Failure |
Device: Remon ImPressure implantable pulmonary artery pressure monitor |
Study Type: | Interventional |
Study Design: | Diagnostic, Non-Randomized, Open Label, Single Group Assignment |
Estimated Enrollment: | 40 |
Study Start Date: | August 2006 |
Estimated Primary Completion Date: | August 2008 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
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1: Experimental |
Device: Remon ImPressure implantable pulmonary artery pressure monitor
Remon ImPressure implantable pulmonary artery pressure monitor responding to ultrasonic signal.
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Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Responsible Party: | Boston Scientific Corporation Cardiac Rhythm Management ( Jeffrey Von Arx, Ph.D./Director, Technology Research ) |
Study ID Numbers: | PAPIRUS II |
Study First Received: | January 4, 2008 |
Last Updated: | June 22, 2009 |
ClinicalTrials.gov Identifier: | NCT00604903 History of Changes |
Health Authority: | Germany: Federal Institute for Drugs and Medical Devices |
Heart Failure Heart Diseases |
Heart Failure Heart Diseases Cardiovascular Diseases |