At a glance

ClinicalIndex Comparison Record

N/ACompleted· 12 enrolled

Drug / intervention

Glucose Sensordevice

Likely dose

Not stated in record

Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02614768

NCT02614768N/ACompleted

Compare CT.gov

Standardized Evaluation of Subcutaneous Glucose Monitoring Systems Under Routine Environmental Conditions

Medical University of Graz·interventional·Posted Nov 25, 2015·Updated May 6, 2023

In Brief

A clinical study evaluating Glucose Sensor for Diabetes Mellitus, Type 1. Completed, enrolled 12 participants.

Detailed Summary

The purpose of this study is to assess accuracy and reliability of the SPIDIMAN continuous glucose monitoring (CGM) sensor system with regard to values as measured by Super GL and compare these results with similar evaluations of the Medtronic MiniMed 640G system, the Abbott FreeStyle Libre Flash Sensor and the DexCom G4 Platinum Sensor in patients with type 1 Diabetes.

Study Details

Study Typeinterventional

Allocation--

Masking--

Primary Purpose--

ConditionsDiabetes Mellitus, Type 1

Countries--

Collaborators--

Timeline

N/ACompletedFinished

20162017201820192020202120222023202420252026

Enrollment StartJul 2015

Primary CompletionAug 2015

Study CompletionSep 2015

First PostedNov 2015

TodayJul 2026

First PostedNov 25, 2015

Enrollment StartJul 1, 2015

Primary CompletionAug 1, 2015

Study CompletionSep 1, 2015

TodayJul 2, 2026

Enrollment to primary: 1 monthPosted 10.6 years ago

Interventions

Glucose Sensordevice

The investigational intervention is CGM monitoring using four different CGM systems. Three of the four CGM devices which are used will be CGM systems which have received conformité européenne (CE) certification (Dexcom G4 Platinum, Medtronic MiniMed 640G system, Abbott FreeStyle Libre Flash). The SPIDIMAN sensor will be used for the first time in human subjects, does not yet have received CE certification and will be given an identifying label in addition to being labelled "for investigative use only".