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COMPLETED

CGM in Patients With ED's

NCT05603481 · View on ClinicalTrials.gov ↗

Study Summary

To determine the accuracy of continuous glucose monitoring (CGM) with point of care (POC) fingerstick glucose monitoring and venous blood glucose in patients with eating disorders, specifically anorexia nervosa, restricting subtype (AN-R); avoidant/restrictive food intake disorder (ARFID); and anorexia nervosa, binge/purge subtype (AN-BP).

Interventions

  • DEVICE Continuous Glucose Monitor

Study Locations (1)

Colorado

  • Denver Health and Hospital Authority — Denver

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2023-05-09
Est. Completion 2024-07-02

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05603481

The ClinicalTrials.gov registry entry for NCT05603481 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Denver Health and Hospital Authority, which has 52 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Avoidant Restrictive Food Intake Disorder appearing as the primary indexed condition, and to 1 intervention — of which Continuous Glucose Monitor is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05603481 reports 1 study location spanning 1 distinct geographic area — top geographies include Colorado. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05603481 about?

NCT05603481 is a clinical study titled "CGM in Patients With ED's". To determine the accuracy of continuous glucose monitoring (CGM) with point of care (POC) fingerstick glucose monitoring and venous blood glucose in patients with eating disorders, specifically anorexia nervosa, restricting subtype (AN-R); avoidant/restrictive food intake disorder (ARFID); and anore...

What is the current status of trial NCT05603481?

This trial is currently completed. The enrollment target is 50 participants. The study started on 2023-05-09. Estimated completion is 2024-07-02.

What conditions does trial NCT05603481 study?

This clinical trial studies the following conditions: Avoidant Restrictive Food Intake Disorder, Anorexia Nervosa, Binge Eating/Purging Type, ARFID, Anorexia Nervosa Restricting Type. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05603481?

The interventions under investigation include: Continuous Glucose Monitor (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05603481?

This trial is sponsored by Denver Health and Hospital Authority, which has 52 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05603481 being conducted?

This trial has 1 study location across Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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