Clinical Trials Directory

Trials / Completed

CompletedNCT04594577

Clinical Validation of the Fluispotter System for Serial Sampling of Venous Dried Blood Spots

The Clinical Validation of Fluispotter®, a Novel Automated Body-worn System for Serial Sampling of Venous Dried Blood Spots

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
22 (actual)
Sponsor
Fluisense ApS · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

This is a prospective, single-centre, non-comparative, non-randomized, open label, clinical investigation of the clinical performance and safety of Fluispotter. The main aim is to validate the clinical performance and safety of the body-worn Fluispotter system used for automated extraction, collection and storage of 20 dried venous dried blood spot samples of 10 µl over the course of 20 hours.

Conditions

Interventions

TypeNameDescription
DEVICEFluispotterFluispotter automated blood sampling system applied for venous blood sampling of 20 10 μL samples in a 20 hours sampling session.

Timeline

Start date
2021-01-27
Primary completion
2021-03-22
Completion
2021-03-22
First posted
2020-10-20
Last updated
2021-05-27

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT04594577. Inclusion in this directory is not an endorsement.

Clinical Validation of the Fluispotter System for Serial Sampling of Venous Dried Blood Spots (NCT04594577) · Clinical Trials Directory