Determination of risk factors of ventricular arrhythmias (VAs) after implantation of
continuous flow left ventricular assist device in order to characterize which patient
requires ICD implantation in primary prevention.
Other: Implantable cardioverter-defibrillator
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Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT02873169
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Patient above 18 years old
Patients with CF-LVAD with or without ICD
Patients subject to major legal protection (safeguarding justice, guardianship, trusteeship), persons deprived of liberty
All locations for NCT02873169
CHU de Bordeaux
Bordeaux, France, 33600
Hospices Civils de Lyon - Hôpital Louis Pradel
Bron, France, 69677
CHU de Caen
CHU Clermont Ferrand
Clermont Ferrand, France, 63003
Hôpital Henri Mondor
Créteil, France, 94010
Dijon, France, 21079
CHU de Grenoble
Grenoble, France, 38700
Centre chirurgical Marie-Lannelongue
Le Plessis-Robinson, France, 92350
CHRU de Lille
Lille, France, 59037
AP-HM - Hôpital de la Timone
Marseille, France, 13385
CHRU de Montpellier
Montpellier, France, 34295
Nancy, France, 54500
Nantes, France, 44000
Hôpital Européen Georges Pompidou
Paris, France, 75015
APHP - Hôpital Bichat
CHU de Rennes
Rennes, France, 35033
CHU de Rouen
Rouen, France, 76000
CHU de Strasbourg
Strasbourg, France, 67091
CHU de Toulouse
CHRU de Tours
Tours, France, 37170
View full eligibility
Tris trial is registered with FDA with number: NCT02873169. The sponsor of the trial is Rennes University Hospital and it is looking for 681 volunteers for the current phase.
Official trial title: Interest of Implantable Cardioverter-defibrillator in Primary Prevention in Patient With Continuous Flow Left Ventricular Assist Device (CF-LVAD)
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