Observation of Clinical Routine Care for Heart Failure Patients Implanted With BIOTRONIK CRT Devices
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- STATUS
- Recruiting
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- End date
- Nov 25, 2024
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- participants needed
- 3000
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- sponsor
- Biotronik SE & Co. KG
Andreas Peth, Dr.
Primary Contact
CH de Valence (0.0 mi away) Contact
+86 other locationSummary
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.
Details
| Treatment | Cardiac resynchronization therapy (CRT) |
|---|---|
| Clinical Study Identifier | NCT03366545 |
| Sponsor | Biotronik SE & Co. KG |
| Last Modified on | 25 October 2020 |
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