I50.1
Conditions
Interventions
Group 1: CRT patients, measurement of LV dP/dt in different pacing modes
Sponsors
Uniklinik Freiburg
Abteilung Kardiologie und Angiologie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: CRT indication according to guidelines, sinus rhythm, informed consent
Exclusion criteria
Exclusion criteria: no consent permanent atrial fibrillation implanted pacemaker or defibrillator severe aortic stenosis age < 18 years pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Identification of optimal pacing site according to invasive hemodynamic monitoring (LV dP/dt) | — |
Secondary
| Measure | Time frame |
|---|---|
| Clinical outcome at 6 months | — |
Countries
Germany
Contacts
Public ContactStefan Asbach
Uniklinik Freiburg
Outcome results
None listed