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SonR Based Stimulation-VECtor OPTimisation in CRT Patients

NCT03092349 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2019-02-06

No results posted yet for this study

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.

Conditions

  • Cardiac Resynchronization Therapy

Interventions

DEVICE

Vector optimisation

Evaluation of hemodynamically best LV Stimulation vector and device programming according to measurements

Sponsors & Collaborators

  • Heart and Diabetes Center North-Rhine Westfalia

    lead OTHER

Principal Investigators

  • Klaus-Jürgen Gutleben, MD · Clinic for Cardiology, Heart and Diabetes Center North Rhine-Westphalia

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-31
Primary Completion
2018-12-31
Completion
2018-12-31

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03092349 on ClinicalTrials.gov