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Device
iGlucose Smart Meter System for Diabetes in Pregnancy (iGlucose Trial)
N/A
Recruiting
Research Sponsored by The University of Texas Health Science Center, Houston
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
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
Timeline
Screening 3 weeks
Treatment Varies
Follow Up perinatal to postpartum (32 weeks)
Awards & highlights
iGlucose Trial Summary
This trial will investigate whether making it easier for women with diabetes to track their blood sugar levels during pregnancy through automated monitoring will improve clinical outcomes.
Eligible Conditions
- Diabetes in Pregnancy
- Gestational Diabetes
- Type 2 Diabetes
iGlucose Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowiGlucose Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ at delivery
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~at delivery
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Anemia, Neonatal
# of neonates who where Small for gestational age (SGA)
Neonatal gestational age at delivery
+2 moreSecondary outcome measures
Average Neonatal Weight
Effect of SMBG checks on pregnancy
Maternal # of Hypoglycemia events (<60 mg/dl)
+7 moreiGlucose Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: iGlucose Smart MeterExperimental Treatment1 Intervention
Group II: Rx glucose meterPlacebo Group1 Intervention
Find a Location
Who is running the clinical trial?
The University of Texas Health Science Center, HoustonLead Sponsor
902 Previous Clinical Trials
320,921 Total Patients Enrolled
Smart Meter CorporationIndustry Sponsor
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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