Actively Recruiting

Age: 2Years +
All Genders
Healthy Volunteers
NCT06483945

Dexcom Continuous Glucose Monitoring System Use in aReal-World, Global Registry (Dexcom Global Registry)

Led by DexCom, Inc. · Updated on 2024-07-03

5000

Participants Needed

2

Research Sites

226 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

"To evaluate the use of the Dexcom CGM System when used according to approved commercial labeling during standard clinical use and its impact on intended users in a real-world setting"

CONDITIONS

Official Title

Dexcom Continuous Glucose Monitoring System Use in aReal-World, Global Registry (Dexcom Global Registry)

Who Can Participate

Age: 2Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Meets Dexcom CGM System Indications for Use per approved commercial labeling
  • Has at least one Hemoglobin A1c measurement within 3 months prior to starting Dexcom CGM System use, at least 3 months after any prior CGM use
  • Willing and able to use Dexcom CGM System according to approved product labeling
  • Willing and able to complete patient reported outcome assessments and surveys
  • Willing and able to comply with the study protocol
  • Willing and able to comply with provider requirements for at least two visits per year
  • Provides written informed consent or is enrolled under an IRB/EC approved waiver of consent
Not Eligible

You will not qualify if you...

  • Contraindicated for Dexcom CGM System use per approved commercial labeling
  • Considered unsuitable candidate by the Investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Institute of Endocrinology Diabetes, Health & Hormones

Stockbridge, Georgia, United States, 30281

Actively Recruiting

2

Palm Research Center

Las Vegas, Nevada, United States, 89148

Actively Recruiting

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Research Team

S

Stayce Beck, PhD

CONTACT

K

Kathleen Hurst

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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