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Clinical Trial Summary

The purpose of this study is to evaluate if in patients with gestational diabetes (GDM), adherence to postprandial glucose monitoring differs when performed 1-hour versus 2-hours after eating. The primary objective of this study is to evaluate difference in rate of adherence (binary outcome defined as <80% or ≥80% of glucose log completed) between gestational diabetics who perform 1-hour versus 2-hour postprandial blood glucose testing.


Clinical Trial Description

Consented patients who are diagnosed with gestational diabetes will be randomized to either 1-hour or 2-hour postprandial blood glucose monitoring. A retrospective chart review from July 2020 until study commencement for patients from the same clinic will be used as a historical control group. This study will assess differences in adherence to testing. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05062460
Study type Interventional
Source Weill Medical College of Cornell University
Contact
Status Enrolling by invitation
Phase N/A
Start date September 2021
Completion date July 2022

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