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Clinical Trial Summary

The primary aim of the present study is to investigate whether the optimisation of LVSV in addition to the optimisation of AV-D and VV-D when using the device-based sensor technology mentioned above results in an improved clinical outcome of CRT. Moreover, noninvasive measurements are intended to evaluate hemodynamic differences between the different stimulation configurations using the Finapres® method.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Cardiac Resynchronization Therapy

NCT number NCT03092349
Study type Observational
Source Heart and Diabetes Center North-Rhine Westfalia
Contact
Status Terminated
Phase
Start date January 2017
Completion date December 31, 2018

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