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NCT07459582 · ClinicalTrials.gov registry record
Accuracy of Home Lactate Meter and Accu-chek Glucometer in Patients With Glycogen Storage Disease
A clinical trial of Glycogen Storage Disease Type Ia and Glycogen Storage Disease Type I, sponsored by Connecticut Children's Medical Center.
- Recruiting
- Registry status
- 10
- Enrollment target
- 1
- Study location
NCT07459582 is a study of Glycogen Storage Disease Type Ia and Glycogen Storage Disease Type I that is actively recruiting participants, run by Connecticut Children's Medical Center. The registered enrollment target is 10 participants, below the 49-participant average among 5 other Glycogen Storage Disease Type Ia trials with a reported enrollment target (80% lower). The trial reports 1 study location across 1 state.
The verdict
NCT07459582, a study of Glycogen Storage Disease Type Ia and Glycogen Storage Disease Type I, is actively recruiting participants, sponsored by Connecticut Children's Medical Center.
- RECRUITING
- Registry status
- 10 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this study is to determine if the Lactate Plus meter is accurate compared to lab lactate levels, and to determine if the Accu chek guide glucometer is accurate compared to lab serum glucose levels in patients with Glycogen Storage Disease Types Ia, Ib and XI. To determine this, patient's will have a one-time planned admission to Connecticut Children's for approximately 8 hours and receive hourly blood draws as well as finger-sticks.
Conditions Studied
Interventions
- OTHER Lactate Meter
- DEVICE Accu Chek
Study Locations (1)
Connecticut
- Connecticut Children's - Hartford
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2026-03 |
| Est. Completion | 2027-12 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07459582
The ClinicalTrials.gov registry entry for NCT07459582 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 49-participant average among 5 other Glycogen Storage Disease Type Ia trials with a reported enrollment target (80% lower). The listed sponsor is Connecticut Children's Medical Center, which has 55 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Glycogen Storage Disease Type Ia appearing as the primary indexed condition, and to 2 interventions - of which Lactate Meter is the first listed.
NCT07459582 reports 1 study location spanning 1 distinct geographic area - top geographies include Connecticut.
Frequently Asked Questions
What is clinical trial NCT07459582 about?
NCT07459582 is a clinical study titled "Accuracy of Home Lactate Meter and Accu-chek Glucometer in Patients With Glycogen Storage Disease". The goal of this study is to determine if the Lactate Plus meter is accurate compared to lab lactate levels, and to determine if the Accu chek guide glucometer is accurate compared to lab serum glucose levels in patients with Glycogen Storage Disease Types Ia, Ib and XI. To determine this, patient'...
What is the current status of trial NCT07459582?
This trial is currently recruiting. The enrollment target is 10 participants. The study started on 2026-03. Estimated completion is 2027-12.
What conditions does trial NCT07459582 study?
This clinical trial studies the following conditions: Glycogen Storage Disease Type Ia, Glycogen Storage Disease Type I, Glycogen Storage Disease Type IB, Glycogen Storage Disease Xi.
What interventions are being tested in trial NCT07459582?
The interventions under investigation include: Lactate Meter (OTHER), Accu Chek (DEVICE).
Who is sponsoring clinical trial NCT07459582?
This trial is sponsored by Connecticut Children's Medical Center, which has 55 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07459582 being conducted?
This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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