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NCT06419803 · ClinicalTrials.gov registry record · NA
Strict Versus Permissive Thresholds for Initiation of Pharmacotherapy in Gestational Diabetes (START 2)
A NA study of Pregnancy Related and Gestational Diabetes, sponsored by Thomas Jefferson University.
- Recruiting
- Registry status
- NA
- Development phase
- 430
- Enrollment target
- 2
- Study locations
NCT06419803 is a NA study of Pregnancy Related and Gestational Diabetes that is actively recruiting participants, run by Thomas Jefferson University. The registered enrollment target is 430 participants, below the 1,959-participant average among 99 other Pregnancy Related trials with a reported enrollment target (78% lower). The trial reports 2 study locations across 2 states.
The verdict
NCT06419803, a NA study of Pregnancy Related and Gestational Diabetes, is actively recruiting participants, sponsored by Thomas Jefferson University.
- RECRUITING
- Registry status
- NA
- Development phase
- 430 participants
- Enrollment target
- 2
- Study locations
Study Summary
The aim of our study is to compare neonatal and maternal outcomes using different thresholds for the initiation and titration of pharmacotherapy for gestational diabetes (GDM). Our goal is to compare a Strict and permissive threshold. The Strict study arm target range will be 65-120 mg/dL, with time in range goal of 70%. The permissive study arm target range will be 65-140 mg/dL, with target time in range goal of 70%.
Conditions Studied
Interventions
- DRUG Insulin
Study Locations (2)
New York
- University of Rochester Medical Center - Rochester
Pennsylvania
- Thomas Jefferson University - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 430 participants |
| Start Date | 2024-09-01 |
| Est. Completion | 2026-05 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06419803
The ClinicalTrials.gov registry entry for NCT06419803 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 430 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,959-participant average among 99 other Pregnancy Related trials with a reported enrollment target (78% lower). The listed sponsor is Thomas Jefferson University, which has 292 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Pregnancy Related appearing as the primary indexed condition, and to 1 intervention - of which Insulin is the first listed.
NCT06419803 reports 2 study locations spanning 2 distinct geographic areas - top geographies include New York, Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT06419803 about?
NCT06419803 is a clinical study titled "Strict Versus Permissive Thresholds for Initiation of Pharmacotherapy in Gestational Diabetes (START 2)". The aim of our study is to compare neonatal and maternal outcomes using different thresholds for the initiation and titration of pharmacotherapy for gestational diabetes (GDM). Our goal is to compare a Strict and permissive threshold. The Strict study arm target range will be 65-120 mg/dL, with time...
What is the current status of trial NCT06419803?
This trial is currently recruiting. It is a NA study. The enrollment target is 430 participants. The study started on 2024-09-01. Estimated completion is 2026-05.
What conditions does trial NCT06419803 study?
This clinical trial studies the following conditions: Pregnancy Related, Gestational Diabetes.
What interventions are being tested in trial NCT06419803?
The interventions under investigation include: Insulin (DRUG).
Who is sponsoring clinical trial NCT06419803?
This trial is sponsored by Thomas Jefferson University, which has 292 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06419803 being conducted?
This trial has 2 study locations across New York, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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