Optimization of CRT Using an ECG Vest
Completed · Not applicable
Conditions studied: Heart Failure
In brief
Despite advancements in implant technology and various techniques of optimization, there is still around 30% non-responder rate to cardiac resynchronization therapy (CRT). This study will assess the potential benefit of a body surface mapping technology to optimize CRT devices in the chronic sub-optimal responder setting.
Key facts
- Study ID
- NCT02699944
- Run by
- Alan J. Bank, MD
- People needed
- 56
- Starts
- 2015-11-01
- Expected to finish
- 2021-08-17
- Last updated by the study team
- 2021-09-23
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients (or their legal guardian) must be willing to provide Informed Consent and a data privacy (HIPPA) authorization
- Patient is or will be followed clinically in the UHVC CRT Optimization Clinic
- Patient has been implanted with a CRT device for at least 6 months
- Patient received an echocardiogram prior to CRT implant
- Patients must be ≥ 18 years of age
You may not qualify if…
- Patient's EF is currently ≥ 50%
- Patients who are pregnant
- Patient has unhealed / open wounds on the torso and/or has a history of severe allergic reactions from ECG gel / electrode glue
Where it is running
- United Heart & Vascular Clinic — Saint Paul, Minnesota, United States
Full record on ClinicalTrials.gov
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