Type 2 Diabetes Clinical Trial
Official title:
Noninvasive Screening for Early Evidence of Diabetes With SCOUT DS
The study will complete up to 500 subjects across 9 clinical sites to evaluate the precision
and accuracy of SCOUT DS (Diabetes Screening) subjects at risk for type 2 diabetes. The
study will involve up to two unique Scout devices at each clinical site. Each site will
initially contain only a CS-1 (Commercial SCOUT 1) "A" for collection of data. As they
become available, CS-1 "B"s operating with latest version of SCOUT software will be shipped
to each site.
The NSEEDS study will enroll patients at-risk for type 2 diabetes who meet the study
inclusion criteria (and do not meet one or more of the exclusion criteria) at approximately
9 clinical sites distributed across the United States. Eligible subjects must be at least 18
years old, not have an existing diagnosis of diabetes and, if less than 45 years old, must
have a body mass index (BMI) ≥ 25 and at least one other risk factor for type 2 diabetes.
The data will be collected and a partial area under the receiver operator curve (pAUC) will
be computed via the method of moments between the 20% and 50% false positive rates based on
the first valid Scout "A" measurement for each patient. The impaired glucose tolerance
status will be determined by the average of the two hour, post challenge plasma glucose
samples measured at the central laboratory. This will be compared to 1000 bootstrap
re-samplings of the calibration data pulling a cohort that matches that collected during
this study. A test will be conducted to assure that the SCOUT performance lies within a 95%
empirical confidence interval based on the bootstrap re-sampling.
n/a
Observational Model: Cohort, Time Perspective: Prospective
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