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Clinical Trials/NCT02929654
NCT02929654
Completed
Not Applicable

Assessment of Blood Glucose Monitoring Devices With New Insight Features

LifeScan3 sites in 1 country267 target enrollmentOctober 1, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Diabetes Mellitus
Sponsor
LifeScan
Enrollment
267
Locations
3
Primary Endpoint
A1c change from baseline after 12 weeks
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

To investigate whether novel insight features in new BGMs can improve glycemic control.

Registry
clinicaltrials.gov
Start Date
October 1, 2016
End Date
June 22, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Sponsor
LifeScan
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

A1c change from baseline after 12 weeks

Time Frame: 12 weeks

A1c change from baseline after 12 weeks in subjects using BGMs with color range indicator and/or pattern messaging tools (i.e., OneTouch Verio® Flex and OneTouch Verio® combined) compared to subjects with either T1 or T2DM using their current BGM, i.e., without color range indicator and/or pattern messaging tools.

Study Sites (3)

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