Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
150 participants
OBSERVATIONAL
2014-06-30
2014-12-31
Brief Summary
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This evaluation will also collect data from a YSI 2300 Stat Plus Glucose Analyzer reference glucometer. The YSI 2300 Stat Plus Glucose Analyzer will be used as the "gold" standard with all results compared to the YSI results.
Detailed Description
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Each subject selected for the comparison evaluation will perform their own fingerstick and test on their subject device following device instructions. A trained technician will perform a fingerstick on the subject immediately after and perform the test on the same device. Separate results will be recorded by subject and technician. A trained technician will take another blood sample, within as short of a time as practicable, for a glucose assay on the YSI 2300 Stat Plus Glucose Analyzer.
Conditions
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Keywords
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Study Design
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CASE_ONLY
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
2. Is the subject able to provide legal, written informed consent?
3. Is the subject willing to have fingersticks for blood glucose determination?
4. Does the subject show an ability and willingness to follow directions of the Investigator and staff?
5. Is the subject 18 years of age or older?
6. Does the subject have a hematocrit value in the range of 20-60?
Exclusion Criteria
2. Is the subject currently participating in another clinical study of an investigational device or drug?
3. Is the subject unwilling or unable to provide concurrent blood glucose level determinations with the YOFiMeter whenever blood glucose levels are determined at the Investigator's site?
4. Is the subject, or a family member, employed by a company that develops or markets blood glucose level determining devices?
5. Does the subject have any other condition or finding, which in the opinion of the investigator would make the subject unsuitable for enrollment, or could interfere with the subject participating in and completing the protocol?
6. Is the subject unwilling or unable to provide Informed Consent (IC)?
18 Years
ALL
Yes
Sponsors
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YofiMeter, LLC
INDUSTRY
Responsible Party
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Principal Investigators
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Timothy Bailey, MD
Role: PRINCIPAL_INVESTIGATOR
AMCR Institute
Locations
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Profil Institute for Clinical Research
Chula Vista, California, United States
AMCR Institute
Escondido, California, United States
Tri City Endocrinology
Oceanside, California, United States
Countries
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Other Identifiers
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YOFiMeter 2013-1
Identifier Type: -
Identifier Source: org_study_id