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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorThe University of Texas Health Science Center, Houston

About this trial

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

Qualifiers

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

Disqualifiers

Patients with Type 1 diabetes

Patients with fetal major congenital abnormalities

Patients identified/referred after 30.6 weeks

Trial design

Treatments tested in this trial

  • iGlucose Smart Meter System
  • Routine Care-RX meter

Treatment groups

200 Participants
are divided into 2 treatment groups

Sponsors and collaborators