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COMPLETED

Development of a Novel Method to Measure Insulin Sensitivity in Humans: A Pilot Study

NCT04774081 · View on ClinicalTrials.gov ↗

Study Summary

This study will determine whether the ratio between 24h C-peptide urinary excretion rate and average 24h circulating glucose represent a good correlate of what is measured by the gold standard, i.e. M (glucose disposal rate) from a euglycemic-hyperinsulinemic clamp

Conditions Studied

Interventions

  • DEVICE 24h Continuous glucose monitoring and urinary C-peptide collection

Study Locations (1)

Louisiana

  • Pennington Biomedical Research Center — Baton Rouge

Trial Details

FieldValue
Enrollment Target 13 participants
Start Date 2021-02-08
Est. Completion 2022-02-21

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04774081

The ClinicalTrials.gov registry entry for NCT04774081 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 13 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pennington Biomedical Research Center, which has 142 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Insulin Sensitivity appearing as the primary indexed condition, and to 1 intervention — of which 24h Continuous glucose monitoring and urinary C-peptide collection 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: NCT04774081 reports 1 study location spanning 1 distinct geographic area — top geographies include Louisiana. 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 NCT04774081 about?

NCT04774081 is a clinical study titled "Development of a Novel Method to Measure Insulin Sensitivity in Humans: A Pilot Study". This study will determine whether the ratio between 24h C-peptide urinary excretion rate and average 24h circulating glucose represent a good correlate of what is measured by the gold standard, i.e. M (glucose disposal rate) from a euglycemic-hyperinsulinemic clamp

What is the current status of trial NCT04774081?

This trial is currently completed. The enrollment target is 13 participants. The study started on 2021-02-08. Estimated completion is 2022-02-21.

What conditions does trial NCT04774081 study?

This clinical trial studies the following conditions: Insulin Sensitivity. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04774081?

The interventions under investigation include: 24h Continuous glucose monitoring and urinary C-peptide collection (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04774081?

This trial is sponsored by Pennington Biomedical Research Center, which has 142 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04774081 being conducted?

This trial has 1 study location across Louisiana. 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