Near-Infrared Spectroscopy for Blood Glucose Measurements

NCT ID: NCT01168115

Last Updated: 2010-07-22

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-01-31

Study Completion Date

2008-12-31

Brief Summary

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The purpose of this study is to evaluate the performance of a near-infrared transmission measurement in blood samples collected from healthy volunteers. We propose that NIR spectroscopic blood glucose measurements in healthy patients are as accurate as handheld glucometers and a Yellow Springs Instrument (YSI). We will also evaluate in vitro blood samples spiked with pharmacological interferents to test if the spectroscopic glucose measurement is affected by common medications.

Detailed Description

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Luminous Medical is developing an automated glucose measurement system that addresses the rapidly growing clinical demand for tight glycemic control in the intensive care unit (ICU), operating room (OR), and intermediate care units. The system automatically measures glucose and other analytes by spectroscopically analyzing blood as it passes through a disposable Sensor Set. Our unique optical measurement does not chemically interact with blood, is insensitive to sensor fouling, and, unlike a biosensor, does not require frequent recalibration.

Conditions

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Healthy

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

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Inclusion Criteria

* Males and females between the ages of 18 and 65
* Healthy
* Not currently pregnant
* Hematocrit \>38%

Exclusion Criteria

* Pregnancy (Self Reported)
* Females that have given birth 6 weeks prior (self reported)
* Anemia (hematocrit \<38%) Hematocrit is checked via a capillary fingerstick and a blood hematocrit reader.
* Under the age of 18 or over the age of 65.
* Diagnosed with Type I or II Diabetes (Self-Reported).
* Donated blood (\>25 mls) in the last 8 weeks
* Heart rate \>100 beats per minute
* Weigh less than 110 lbs.
* Currently taking anticoagulants (ex: coumadin)
* Abnormal blood pressure (diastolic \>90)
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Luminous Medical

INDUSTRY

Sponsor Role collaborator

InLight Solutions

INDUSTRY

Sponsor Role lead

Responsible Party

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InLight

Principal Investigators

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Mark Rohrscheib, M.D.

Role: PRINCIPAL_INVESTIGATOR

UNMHSC

Locations

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InLight Solutions

Albuquerque, New Mexico, United States

Site Status

Countries

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United States

Related Links

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Other Identifiers

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ILS-07-386

Identifier Type: -

Identifier Source: org_study_id

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