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NCT04840446 | Completed | Diabetes


Evaluation of Modified Adhesives With Dexcom G6 Sensor
Sponsor:

DexCom, Inc.

Brief Summary:

The purpose of the study is to collect and compare information on the performance of CGM adhesives in adults.

Condition or disease

Diabetes

Intervention/treatment

Dexcom Continuous Glucose Monitoring System

Study Type : Observational
Estimated Enrollment : 80 participants
Official Title: Evaluation of Modified Adhesives With Dexcom G6 Sensor
Actual Study Start Date : February 8, 2021
Estimated Primary Completion Date : March 16, 2021
Estimated Study Completion Date : March 19, 2021

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: All
Accepts Healthy Volunteers: Accepts Healthy Volunteers
Criteria
Inclusion Criteria
  • Age 18 or older;
  • No previously self-reported adhesive reactions to the any continuous glucose monitor (CGM);
Exclusion Criteria
  • Extensive skin changes/diseases that preclude wearing the required number of devices (e.g., history of severe reactions from adhesive wear, extensive psoriasis, recent burns or severe sunburn, extensive eczema, extensive scarring, extensive tattoos, dermatitis herpetiformis) at the proposed wear sites;
  • Current or anticipated use of systemic corticosteroids (oral, injectable, or intravenous)

Evaluation of Modified Adhesives With Dexcom G6 Sensor

Location Details


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Evaluation of Modified Adhesives With Dexcom G6 Sensor

How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations


Not yet recruiting

United States, Florida

Jaeb Center for Health Research

Tampa, Florida, United States, 33647

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