A Performance Evaluation of the Enlite 3 Sensor

Withdrawn before enrolling · Not applicable

Conditions studied: Type 1 Diabetes

In brief

The purpose of this study is to support the use of the Enlite 3 sensor in arm and thigh in subjects age 14 - 75 years and provide additional characterization of the Enlite 3 sensor performance in arm in subjects age 14 - 75 years.

Key facts

Study ID: NCT02649010
Run by: Medtronic MiniMed, Inc.
People needed: 0
Starts: 2016-01-01
Expected to finish: 2016-05-01
Last updated by the study team: 2016-06-23

Who can join

Age: 14 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Subject is 14 - 75 years of age at time of screening.
A clinical diagnosis of type 1 or 2 diabetes for a minimum of 9 months duration as determined via medical record or source documentation by an individual qualified to make a medical diagnosis
Adequate venous access as assessed by investigator or appropriate staff
Subjects participating in the high and low glucose challenges must have an established insulin carbohydrate ratio(s) and insulin sensitivity ratio. (The term "established" refers to a ratio that has been previously defined and tested prior to screening visit). Subjects without established ratios may participate under observation only.

You may not qualify if…

Subject will not tolerate tape adhesive in the area of Enlite 3 Sensor placement as assessed by qualified individual.
Subject has any unresolved adverse skin condition in the area of Enlite 3 Sensors or device placement (e.g., psoriasis, rash, Staphylococcus infection)
Subject is actively participating in an investigational study (drug or device) wherein they have received treatment from an investigational study (drug or device) in the last 2 weeks
Subject is female and has a positive pregnancy screening test
Females of child bearing age and who are sexually active should be excluded if they are not using a form of contraception deemed reliable by investigator.
Subject is female and plans to become pregnant during the course of the study
Subject has had a hypoglycemic seizure within the past 6 months.
Subject has had hypoglycemia resulting in loss of consciousness within the past 6 months prior to screening visit.
Subject has had an episode of diabetic ketoacidosis (DKA) within the past 6 months prior to screening visit.
Subject has a history of a seizure disorder.
Subject has central nervous system or cardiac disorder resulting in syncope.
Subject has a history of myocardial infarction, unstable angina, coronary artery bypass surgery, coronary artery stenting, transient ischemic attack (TIA), cerebrovascular accident (CVA), angina, congestive heart failure, ventricular rhythm disturbances or thromboembolic disease.
Subject has a hematocrit(Hct) lower than the normal reference range.
Subject has a history of adrenal insufficiency

Where it is running

Diablo Clinical Research — Walnut Creek, California, United States
Rainier Clinical Research Center — Renton, Washington, United States

Full record on ClinicalTrials.gov

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