Customer Support Response Study

Withdrawn before enrolling

Conditions studied: Type 2 Diabetes

In brief

The primary objective of the CUSTOM study is to respond to customer support issues (outside of the US) and to assess the impact of a particular treatment or perturbation relative to an initial control measurement. Sequential subject measurements will be analyzed to determine if a given action or condition induces a score shift, an inflation of measurement variance or elevated outlier rates.

Key facts

Study ID

NCT01547403

Run by

VeraLight, Inc.

People needed

0

Starts

2012-08-01

Expected to finish

2013-01-01

Last updated by the study team

2013-01-15

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Males and/or females greater than or equal to 18 years of age

You may not qualify if…

• Have received investigational treatments in the past 14 days
• Have psychosocial issues that interfere with an ability to follow study procedures
• Are known to be pregnant
• Have scars, tattoos, rashes or other disruption/discoloration on the left volar forearm.
• Have been treated on the past month with oral steroid therapy or topical steroids applied to the left forearm. Inhaled steroid therapy is not a basis for exclusion
• Are receiving medications that fluoresce (A list of excluded medications is located in Appendix H)
• Are known to have, or at risk for, photosensitivity reactions (e.g., sensitive to ultraviolet light, or taking medication known to cause photosensitivity)

Where it is running

• VeraLight — Albuquerque, New Mexico, United States

Full record on ClinicalTrials.gov

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