Comparative Evaluation of the FINDER Instrument and FINDER G6PD Cartridge in Adults and Neonates

Completed

Conditions studied: G6PD, G6PD Deficiency

In brief

A prospective clinical study to compare the clinical performance of the FINDER™ Instrument and the G6PD assay to an FDA cleared instrument/reagent combination in adult and neonate populations.

Key facts

Study ID

NCT04146246

Run by

Baebies, Inc.

People needed

119

Starts

2019-11-11

Expected to finish

2020-03-13

Last updated by the study team

2020-11-23

Who can join

Age: 1 and older, up to 100. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Neonates aged >35 gestational weeks or older.
• Adult subjects who are age 18 and older.
• Adult subjects who weigh at least 110 pounds.
• All ethnicities.
• Male and female subjects.

You may not qualify if…

• Adult subjects who weigh less than 110 pounds.
• Subjects with anemia for which an attending physician will not authorize a blood draw.
• Subjects who have received a blood transfusion.
• Subjects who are pregnant.

Where it is running

• Duke Health — Durham, North Carolina, United States
• Wake Med — Raleigh, North Carolina, United States
• University Hospitals Cleveland Medical Center Rainbow Children's Hospital — Cleveland, Ohio, United States

Full record on ClinicalTrials.gov

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