Evaluation of Modified Adhesives With Dexcom G6 Sensor

Dexcom

Status: Completed

Conditions: Diabetes

Treatments: Device: Dexcom Continuous Glucose Monitoring System

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT04840446

PTL-904288

Details and patient eligibility

About

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

Enrollment: 80 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Age 18 or older;
2. No previously self-reported adhesive reactions to the any continuous glucose monitor (CGM);

Exclusion criteria

1. 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;
2. Current or anticipated use of systemic corticosteroids (oral, injectable, or intravenous)