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Clinical Trial Summary

The primary objective of this study is to assess the percentage of time patients were in normal glucose control.


Clinical Trial Description

Retrospective Dexcom G6 iCGM data stored in the Clarity cloud from eligible patients will be accessed and downloaded, stripped of patient-identifying information and provided to the contract research organization (CRO) to review prior to sending to the Sponsor for analysis of glycemic control. The CRO will ensure data shared with the Sponsor is de-identified and transferred over a secure file transfer platform. Further, Remote Site Specialists (RSSs) from the CRO will work with the healthcare providers (HCPs) from participating sites to obtain additional patient data including medical history, prescribed diet, cornstarch/Glycosade use and demographic data directly, if available, from the medical charts and will enter this information into an electronic data capture (EDC) system. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04708015
Study type Observational
Source Ultragenyx Pharmaceutical Inc
Contact
Status Completed
Phase
Start date November 5, 2020
Completion date March 4, 2022

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