Heart Failure Clinical Trial

Metabolic Mapping and Cardiac Resynchronization

Summary

The purpose of this study is to gather information on the safety and effectiveness of cardiac resynchronization therapy (CRT) in patients who have mild heart failure (HF) and left bundle branch block (LBBB).

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

LVEF 35%-50%
NYHA class I-II
QRS duration of ≥120ms
Left bundle branch block (LBBB)
Patient is able to receive a transvenous pectoral CRT implant
Patient is able to sign informed consent
Two echocardiograms are required to confirm a stable reduced LVEF
Patient is on optimal and stable medical therapy (ACE inhibitor or AT1 blocker, beta blocker, etc. over the last 6 months)

Exclusion Criteria:

Advanced comorbid conditions with life expectancy <1 year
Patient is <18 of years of age
Patient has a CRT device
Female patients who is pregnant or not on a reliable form of birth control. Women of childbearing potential are required to have negative pregnancy test within the 7 days prior to device implant
Unwilling or unable to return for required follow-up visits
Patient decides study participation is cost-prohibited

Study is for people with:

Heart Failure

Estimated Enrollment:

100

Study ID:

NCT03420833

Recruitment Status:

Recruiting

Sponsor:

Yong-Mei Cha

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There is 1 Location for this study

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Mayo Clinic in Rochester
Rochester Minnesota, 55905, United States More Info
Brian Liddell
Contact
507-255-0774
[email protected]
Yong-Mei Cha, MD
Principal Investigator

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Estimated Enrollment:

100

Study ID:

NCT03420833

Recruitment Status:

Recruiting

Sponsor:


Yong-Mei Cha

How clear is this clinincal trial information?

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