Point of Service Diabetes Screening Evaluation

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01669616

Acronym

POSSE

Enrollment

667

Registered

2012-08-21

Start date

2012-08-31

Completion date

2013-01-31

Last updated

2013-01-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus, Non-Insulin Dependent

Keywords

Type 2 Diabetes, Adults 18 years and older

Brief summary

The primary objective of the trial is to collect SCOUT DS, random capillary glucose and Hemoglobin A1c measurements from subject 18 years of age or older.

Detailed description

The objectives of this study are to compare the accuracy of SCOUT versus random capillary glucose and several diabetes risk assessment questionnaires for detection of HbA1C-defined dysglycemia.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* 18 years of age or older

Exclusion criteria

* Known to be pregnant (self-reported) * Receiving dialysis or known renal compromise * Known to have photosensitivity * Taking medications that fluoresce * Have scars, any tattoos, rashes or other disruption/discoloration on the left volar forearm

Design outcomes

Primary

Measure	Time frame
To compare the accuracy of SCOUT DS versus random capillary glucose and several diabetes risk assessment questionnaires for detection of HbA1c-defined dysglycemia.	one week

Countries

United States

Outcome results