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UnknownNCT01415544

Comparison of Noninvasive Blood Glucose Concentrations Relative to Finger Capillary Blood Glucose References

An Evaluation and Comparison of Noninvasive Blood Glucose Concentrations Relative to Finger Capillary Blood Glucose References

Status
Unknown
Phase
Study type
Observational
Enrollment
100 (estimated)
Sponsor
InLight Solutions · Industry
Sex
Female
Age
20 Years – 50 Years
Healthy volunteers
Accepted

Summary

The purpose of the study is to prospectively evaluate a noninvasive, near-infrared based method for measuring glucose concentration relative to invasive blood reference measurements. The initial phase of the study will be focused on procurement of the data needed to develop a robust, accurate calibration. The second phase will be focused on performance evaluation of the system.

Detailed description

Currently, individuals with diabetes must use an invasive finger stick methodology for the determination of their blood glucose levels. Although current technology glucose meters use a smaller amount of blood than older generation meters, the pain and inconvenience associated with this invasive measurement is the number one reason cited for inadequate or infrequent blood glucose monitoring. In fact up to 67% of patients with diabetes fail to routinely monitor their blood glucose levels. A survey of 1895 patients showed that finger soreness was the most common reason given for self-reported noncompliance with testing recommendations, followed by pain, inconvenience, fear of needles, and "other" (including cost), (Diabetes Care August 2001 vol. 24 no. 8 1502-1503). The ability to make a painless blood glucose measurement using only light would address the pain and inconvenience issues associated with current technology glucose meters. The initial application of the technology is associated with the monitoring of Gestational Diabetes. The International Association of Diabetes and Pregnancy Study Groups (IADPSG) recently released recommendations for diagnosing gestational diabetes, as well as clarifying the benefits of treatment (Diabetes Care, 2010;33:676-682). The IADPSG cited research that found significant graded relationships between increasing maternal glucose levels and the frequency of four primary and five secondary outcomes. For example, with a 1-standard deviation increase in maternal fasting, 1-hour, and 2-hour plasma glucose levels, there was a corresponding 38%, 46%, and 38% increased risk, respectively, in the primary outcome of birth weight \>90th percentile, and a 5%, 18%, and 16% increased risk, respectively, of the secondary outcome of premature delivery before 37 weeks gestation (N Engl J Med 2008;358:1991-2002).

Conditions

Timeline

Start date
2011-06-01
Primary completion
2012-02-01
Completion
2012-02-01
First posted
2011-08-12
Last updated
2012-02-27

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01415544. Inclusion in this directory is not an endorsement.

Comparison of Noninvasive Blood Glucose Concentrations Relative to Finger Capillary Blood Glucose References (NCT01415544) · Clinical Trials Directory