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COMPLETED NA

Post Approval Study of the Eversense® Continuous Glucose Monitoring

NCT03908125 · View on ClinicalTrials.gov ↗

Study Summary

A Post Approval Study to Evaluate the Long-term Safety and Effectiveness of the Eversense® Continuous Glucose Monitoring (CGM) System over repeat insertion and removal cycles and to demonstrate the long-term safety of the Eversense® CGM System

Interventions

  • DEVICE Eversense® CGM System

Study Locations (17)

Texas

  • Texas Diabetes and Endocrinology — Austin
  • Clinical Research Solution, LLC — Cypress
  • Javara, Inc — Houston
  • Diabetes and Glandular Disease Clinic — San Antonio
  • Consano Clinical Research, LLC — Shavano Park

North Carolina

  • Physicians East — Greenville
  • PMG Research of Wilmington, LLC — Wilmington

California

  • Hoag Memorial Hospital Presbyterian/Mary Dick Allen Diabetes Center — Newport Beach

Colorado

  • Denver Endocrinology, Diabetes & Thyroid Center — Englewood

Florida

  • The Center for Diabetes and Endocrine Care — Fort Lauderdale

Georgia

  • Atlanta Diabetes Associates — Atlanta

Maryland

  • MODEL Clinical research — Baltimore

Michigan

  • Metro Detroit Endocrinology Center — Dearborn

Trial Details

FieldValue
Enrollment Target 273 participants
Start Date 2019-03-19
Est. Completion 2024-02-01
Phase NA

Sponsor

Senseonics

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03908125

The ClinicalTrials.gov registry entry for NCT03908125 describes a study currently listed as completed. It is categorized as NA, 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 273 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Senseonics, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Diabetes Mellitus, Type 2 appearing as the primary indexed condition, and to 1 intervention — of which Eversense® CGM System 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: NCT03908125 reports 17 study locations spanning 12 distinct geographic areas — top geographies include Texas, North Carolina, California. 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 NCT03908125 about?

NCT03908125 is a clinical study titled "Post Approval Study of the Eversense® Continuous Glucose Monitoring". A Post Approval Study to Evaluate the Long-term Safety and Effectiveness of the Eversense® Continuous Glucose Monitoring (CGM) System over repeat insertion and removal cycles and to demonstrate the long-term safety of the Eversense® CGM System

What is the current status of trial NCT03908125?

This trial is currently completed. It is a NA study. The enrollment target is 273 participants. The study started on 2019-03-19. Estimated completion is 2024-02-01.

What conditions does trial NCT03908125 study?

This clinical trial studies the following conditions: Diabetes Mellitus, Type 2, Diabetes Mellitus, Diabetes Mellitus, Type 1. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03908125?

The interventions under investigation include: Eversense® CGM System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03908125?

This trial is sponsored by Senseonics, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03908125 being conducted?

This trial has 17 study locations across California, Colorado, Florida, Georgia, Maryland. 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