180
Participants
Start Date
February 29, 2008
Primary Completion Date
June 30, 2010
Study Completion Date
June 30, 2010
Navigator®
Patients will be encouraged to use the Navigator® all the time and to modify their treatment according to the device measurments. Patients will also follow and educational process in order to adapt insulin doses according to each sensor data
Navigator®
Patients will follow the same educational process as group1 concerning insulin doses adaptation.The duration of the use of the devicewill be determined at the consultation every each 3 months.
Placebo
Patients will have their usual follow up with self-monitoring blood glucose
CHU Sart Tilman Liège, Liège
CHU Marseille Hôpitaux Sud, Marseille
CHU Jean Minjoz, Besançon
CHU Toulouse, Toulouse
Hopital Haut Leveque, Pessac
Chu Montpellier, Montpellier
CHU Rennes, Rennes
University Hospital Grenoble, Grenoble
Hopital Bellevue, Saint-Etienne
CHU Nantes, Nantes
CHU de Reims-Hôpital Américain, Reims
CHU de Reims-Hôpital Robert debré, Reims
CHU Hôpital Jeanne d'Arc, Nancy
CHU Strasbourg, Strasbourg
Hopital Edouard Herriot, Lyon
Hopital Hotel Dieu, Paris
CHU La Pitié Salpetrière, Paris
CHU Robert Debré, Paris
CH SUD Francilien, Corbeil-Essonnes
Collaborators (1)
Abbott
INDUSTRY
Centre d'Etudes et de Recherche pour l'Intensification du Traitement du Diabète
OTHER