Heart Failure Clinical Trial
— MASCOTOfficial title:
Management of Atrial Fibrillation Suppression in AF-HF COmorbidity Therapy
NCT number | NCT00187252 |
Other study ID # | CR03001HF |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | September 2003 |
Est. completion date | June 2008 |
Verified date | February 2019 |
Source | Abbott Medical Devices |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to evaluate whether adding AF Suppression™ to cardiac resynchronization therapy (CRT) improves the prognosis of heart failure patients benefiting from cardiac resynchronization therapy.
Status | Completed |
Enrollment | 380 |
Est. completion date | June 2008 |
Est. primary completion date | June 2008 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - HF patients - New York Heart Association (NYHA) III - IV - Spontaneous QRS =130 ms and/or mechanical interventricular delay > 50 ms - Left ventricular ejection fraction (LVEF) = 35% - Left ventricular end diastolic diameter (LVEDD) = 55 mm - Optimized medical regimen - Age > 18 years Exclusion Criteria: - Unstable angina or acute myocardial infarction (MI) (< 3 months) - Coronary artery bypass grafting (CABG) or percutaneous transluminal coronary angioplasty (PTCA) < 3 months - Life expectancy < 6 months - Permanent AF - Pregnancy |
Country | Name | City | State |
---|---|---|---|
Italy | Clinica Medica Generale e Cardiologia - Ospedale Careggi | Firenze |
Lead Sponsor | Collaborator |
---|---|
Abbott Medical Devices |
Italy,
Padeletti L, Musilli N, Porciani MC, Colella A, Di Biase L, Ricciardi G, Pieragnoli P, Michelucci A, Gensini G. Atrial fibrillation and cardiac resynchronization therapy: the MASCOT study. Europace. 2004 Sep;5 Suppl 1:S49-54. — View Citation
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---|---|---|---|---|
Primary | Prevalence of permanent atrial fibrillation | 2 years |
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