Data Collection Study of Wedge Pressure Data in Patients With CRT-D Devices
Status: | Completed |
---|---|
Conditions: | Cardiology |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/6/2019 |
Start Date: | December 2008 |
End Date: | April 2011 |
zWedge Clinical Feasibility IDE Study
zWedge is a clinical feasibility IDE study. The objective is to characterize the relationship
between intra-thoracic impedance measurements obtained from a CRT-D device and pulmonary
capillary wedge pressure (PCWP) measured via a right heart catheterization (RHC) acutely and
over time.
between intra-thoracic impedance measurements obtained from a CRT-D device and pulmonary
capillary wedge pressure (PCWP) measured via a right heart catheterization (RHC) acutely and
over time.
Intra-thoracic impedance will be obtained at programmed intervals by using an investigational
monitoring feature in the CRT-D device. To obtain impedance values, the device delivers a
sub-threshold impulse that measures the resistance between 2 electrodes.
monitoring feature in the CRT-D device. To obtain impedance values, the device delivers a
sub-threshold impulse that measures the resistance between 2 electrodes.
Inclusion Criteria:
- Have a SJM PROMOTE CRT-D (Model 3207 or other model with similar functioning) system
that was implanted at least 4 months prior to enrollment for an approved indication
per ACC/AHA/HRS guidelines.
- Have the ability to provide written informed consent for study participation and be
willing and able to comply with the prescribed follow-up tests and schedule of
evaluation.
- Have legally marketed bipolar right atrial and true bipolar right ventricular pacing
defibrillation leads, and a legally marketed endocardial bipolar LV lead.
Exclusion Criteria:
- Be less than 18 years of age.
- Have any medical condition that would interfere with intra-thoracic measurements such
as end-stage pulmonary disease, advanced interstitial pulmonary disease, or frequent
episodes of pneumonia.
- Have a contraindication for right heart catheterization.
- Have a contraindication for the delivery of IV Nitroglycerin.
- Be pregnant or planning a pregnancy for the duration of their study participation.
- Be currently participating in a clinical investigation that includes an active
treatment arm.
- Have a life expectancy of less than 12 months due to any condition.
- Be unable to perform the Valsalva maneuver with airway pressure > 40 mm Hg for ≥10
seconds.
- Are pacemaker dependent, where cessation of pacemaker function consistently results in
syncope or ventricular asystole.
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