Trials / Completed
CompletedNCT05062460
Glucose Testing in GDM: Adherence to One- Versus Two-hour Postprandial Glucose Monitoring in Gestational Diabetics
Adherence to One- Versus Two-hour Postprandial Glucose Monitoring in Gestational Diabetics: A Randomized Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 140 (actual)
- Sponsor
- Weill Medical College of Cornell University · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Detailed 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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | 1 hour Blood glucose monitoring | Consented patients who are diagnosed with gestational diabetes will be randomized to 1-hour postprandial blood glucose monitoring. |
| OTHER | 2 hour blood glucose monitoring | Consented patients who are diagnosed with gestational diabetes will be randomized to 2 hour post prandial blood glucose monitoring |
Timeline
- Start date
- 2021-07-15
- Primary completion
- 2024-06-01
- Completion
- 2025-05-01
- First posted
- 2021-09-30
- Last updated
- 2025-05-23
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT05062460. Inclusion in this directory is not an endorsement.