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Clinical Trial Summary

The purpose of this study is to evaluate the performance of an insulin pump controlling algorithm while the subject is under close medical supervision in the Clinical Research Center (CRC) setting.


Clinical Trial Description

This study is a non-randomized, uncontrolled feasibility study that looks to enroll people with type 1 diabetes who are currently using an insulin pump. During the subject's participation, the study staff will closely monitor the study subject in a clinical research center environment for approximately 24 hours, while controller algorithm determined insulin doses are delivered by an insulin pump, and utilizing continuous glucose monitoring results.

Total subject participation approximately 1 week for screening to completion. This includes approximately 24 hours usage of the investigation device in the clinical research center under close medical supervision. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01401751
Study type Interventional
Source Animas Corporation
Contact
Status Completed
Phase N/A
Start date July 1, 2011
Completion date December 1, 2011

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