Changes in Doppler Signals From the Lung Due to Cardiac Resynchronization in Heart Failure Patients
| Status: | Completed |
|---|---|
| Conditions: | Cardiology |
| Therapuetic Areas: | Cardiology / Vascular Diseases |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 4/21/2016 |
| Start Date: | July 2014 |
| End Date: | August 2015 |
Lung Doppler Signals Changes in Response to Cardiac Resynchronization in Heart Failure Patients
Study Purpose and Rationale The purpose of this study is to evaluate the lung Doppler
signals changes during cardiac resynchronization procedure. As the LDS represent the various
mechanical events of cardiac origin it is assumed that they may reflect the relative timing
between contraction of the ventricles and atria and thus serve for effective synchronization
of these activities.
Aim of the study:
The aim of the study is to assess whether the changes in Lung Doppler Signal (LDS) waves'
characteristics will mimic the changes in echocardiographic parameters designed to assess
diastolic inflow and systolic flow in patients undergoing Echo-based CRT optimization.
signals changes during cardiac resynchronization procedure. As the LDS represent the various
mechanical events of cardiac origin it is assumed that they may reflect the relative timing
between contraction of the ventricles and atria and thus serve for effective synchronization
of these activities.
Aim of the study:
The aim of the study is to assess whether the changes in Lung Doppler Signal (LDS) waves'
characteristics will mimic the changes in echocardiographic parameters designed to assess
diastolic inflow and systolic flow in patients undergoing Echo-based CRT optimization.
Inclusion Criteria:
- Male and female patients 18 years or older, who met the indications for cardiac
synchronization therapy (CRT) per the ACCF/AHA guidelines, underwent successful
system implant for more than 3 months, and were referred to the CRT non-responder
clinic at the Ohio State University for CRT- Echo optimization due to absence of
clinical improvement in functional class or ejection fraction after the implant per
the judgment of the referring physician.
Exclusion Criteria:
1. Chronic atrial fibrillation or new cardiac arrhythmias detected at the time of the
visit that are known to affect the response to CRT (Atrial fibrillation,
supraventricular tachycardia, ventricular tachycardia, or frequent premature
ventricular contractions).
2. CRT device malfunction
3. Inadequate CRT programming that has contributed to lack of response to CRT
4. Coronary sinus lead anatomical or electrical malfunctions at the time of the visit
5. Acute systemic illness that can explain their lack of functional improvement (i.e.,
anemia, severe electrolyte imbalance, pneumothorax, pericardial effusion, pneumonia)
6. Inability to sign informed consent
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