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Recruiting NCT04206748

NCT04206748 iGlucose® Remote Patient Monitoring Device as an Adjunct to Routine Glucose Meter Devices for Glycemic Management and Control in Gestational Diabetes

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Clinical Trial Summary
NCT ID NCT04206748
Status Recruiting
Phase
Sponsor The University of Texas Health Science Center, Houston
Condition Gestational Diabetes
Study Type INTERVENTIONAL
Enrollment 200 participants
Start Date 2019-11-12
Primary Completion 2021-11-12

Trial Parameters

Condition Gestational Diabetes
Sponsor The University of Texas Health Science Center, Houston
Study Type INTERVENTIONAL
Phase N/A
Enrollment 200
Sex FEMALE
Min Age 18 Years
Max Age N/A
Start Date 2019-11-12
Completion 2021-11-12
Interventions
iGlucose Smart Meter SystemRoutine Care-RX meter

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Brief Summary

The purpose of this study is to investigate whether automation of glucose monitoring data to facilitate the total number of recommended and completed SMBG checks improve clinical outcomes for women living with gestational and type 2 diabetes during pregnancy? This is a RCT

Eligibility Criteria

Inclusion Criteria * All patients \>/= women 18 years of age with gestational diabetes or type 2 diabetes during pregnancy and identified by the research team and consented before 30.6 weeks. * Non-anomalous singletons * Ability to provide informed consent Exclusion Criteria * Patients with Type 1 diabetes * Patients with fetal major congenital abnormalities * Patients identified/referred after 30.6 weeks

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