Tolerability and Background Fluorescence of the MediBeacon Transdermal GFR Measurement System

Completed · Not applicable

Conditions studied: Acute Kidney Injury

In brief

This study is designed to evaluate background fluorescence of participants of different ages, gender, and skin color. In addition, 48-hour tolerability of the sensor and adhesive will be evaluated.

Key facts

Study ID

NCT03810833

Run by

MediBeacon

People needed

12

Starts

2019-09-16

Expected to finish

2019-09-23

Last updated by the study team

2020-01-10

Who can join

Age: 18 and older, up to 99. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Healthy male and female adults age 18 and older
• 2 age cohorts to be recruited: 18 - 50 years of age and 51+ years or older
• Skin color groups to be recruited in accordance with the Fitzpatrick Skin Scale (I - VI)
• Participants willing to sign the Institutional Review Board (IRB) approved informed consent form prior to the initiation of any study specific procedures.

You may not qualify if…

• History of skin sensitivity to adhesives (e.g. Band-Aids, surgical tape)
• Any characteristics which, in the opinion of the investigator, makes the participant a poor candidate for participation in the clinical trial
• Significant scarring, tattoos or alterations in pigmentation on the standardized sensor locations that would alter sensor readings versus other areas of the skin

Where it is running

• St. Louis Clinical Trials — St Louis, Missouri, United States

Full record on ClinicalTrials.gov

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