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NCT05062460 · ClinicalTrials.gov registry record · NA

Glucose Testing in GDM: Adherence to One- Versus Two-hour Postprandial Glucose Monitoring in Gestational Diabetics

A NA study, sponsored by Weill Medical College of Cornell University.

Completed
Registry status
NA
Development phase
140
Enrollment target

NCT05062460 is a NA study that has completed, run by Weill Medical College of Cornell University. The registered enrollment target is 140 participants.

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The verdict

NCT05062460, a NA study, has completed, sponsored by Weill Medical College of Cornell University.

COMPLETED
Registry status
NA
Development phase
140 participants
Enrollment target

Study 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.

Interventions

  • OTHER 1 hour Blood glucose monitoring
  • OTHER 2 hour blood glucose monitoring

Trial Details

FieldValue
Enrollment Target 140 participants
Start Date 2021-07-15
Est. Completion 2025-05-01
Phase NA

What the Registry Record Tells You About NCT05062460

The ClinicalTrials.gov registry entry for NCT05062460 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 140 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Weill Medical College of Cornell University, which has 701 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which 1 hour Blood glucose monitoring is the first listed.

NCT05062460 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05062460 about?

NCT05062460 is a clinical study titled "Glucose Testing in GDM: Adherence to One- Versus Two-hour Postprandial Glucose Monitoring in Gestational Diabetics". 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...

What is the current status of trial NCT05062460?

This trial is currently completed. It is a NA study. The enrollment target is 140 participants. The study started on 2021-07-15. Estimated completion is 2025-05-01.

What interventions are being tested in trial NCT05062460?

The interventions under investigation include: 1 hour Blood glucose monitoring (OTHER), 2 hour blood glucose monitoring (OTHER).

Who is sponsoring clinical trial NCT05062460?

This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.