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

NCT05062460 is a NA study that has completed, run by Weill Medical College of Cornell University. The registered enrollment target is 140 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

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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.

Primary Outcome

Evaluate 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 finished NCT05062460 record still lists

NCT05062460 is an interventional study that assigns participants to a tested intervention. The registered 140 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower).

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

NCT05062460 does not publish any study locations in the registry export this page uses.

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.

How this trial's enrollment target compares

Where NCT05062460's enrollment target sits among peer trials

140 713th of 2000 higher than 1,281 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05062460, the US trial registry maintained by the National Library of Medicine. NCT05062460 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.