Observation of Clinical Routine Care for Heart Failure Patients Implanted With BIOTRONIK CRT Devices

  • End date
    Nov 25, 2024
  • participants needed
  • sponsor
    Biotronik SE & Co. KG
Updated on 25 October 2020
Andreas Peth, Dr.
Primary Contact
CH de Valence (0.0 mi away) Contact
+86 other location
cardiac resynchronization therapy


The registry is primarily designed to assess outcome, efficacy and residual safety aspects of CRT based on long-term data from an unselected, real-life clinical set-up. Moreover, the observation of the patient status should help to find possible predictors for HF events and to identify areas of improvement for CRT and for CRT device settings.

Treatment Cardiac resynchronization therapy (CRT)
Clinical Study IdentifierNCT03366545
SponsorBiotronik SE & Co. KG
Last Modified on25 October 2020

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Inclusion Criteria

Is your age greater than or equal to 18 yrs?
Gender: Male or Female
Do you have any of these conditions: Heart disease or Cardiac Disease or Congestive Heart Failure or Heart failure?
Planned de novo implantation of or upgrade to a CRT system for treatment according to the intended use
Patient is able to understand the nature of the registry and has provided written informed consent
Patient is willing and able to use the CardioMessenger and accepts the Home Monitoring concept
Remote monitoring using the Home Monitoring platform is planned for the patient

Exclusion Criteria

Standard contraindication for CRT
Already or previously implanted with CRT system
Age < 18 years
Participation in another interventional clinical investigation other than the registry-based trials of BIO|STREAM.HF
Pregnant or breastfeeding
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