Feasibility Study of the JewelPump Version 3

Status Completed

Clinical Trial Summary

The study will be conducted, in cross-over with a time interval of at least 2 days between 2 treatment periods. Patients will be randomized into 2 groups According to the order of the randomization, patients will bear the JewelPump for 5 days, followed by a period of 5 days of treatment with their usual pumps.

Clinical Trial Description

The JewelPump (Debiotech) will be compared to the conventional pumps. Patients will treated with the JewelPump during 5 days, and with their usual pump during 5 other days.

The study will be conduct with 15 patients at the following investigation centers : Corbeil Hospital, CHU of Strasbourg, and CHRU of Marseille. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Type 1 Diabetes

Clinical Trial Details

NCT number	NCT02097316
Study type	Interventional
Source	Centre d’Etudes et de Recherche pour l’Intensification du Traitement du Diabète
Contact
Status	Completed
Phase	Phase 3
Start date	June 2014
Completion date	September 2014

View Details

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