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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04304612
Other study ID # RECHMPL20_0141
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2020
Est. completion date December 30, 2023

Study information

Verified date September 2021
Source University Hospital, Montpellier
Contact Edouard TUAILLON, MD, PhD
Phone 467 338 469
Email e-tuaillon@chu-montpellier.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The consortium will develop a new in vitro diagnostic (IVD) test to screen donated blood for bloodborne infectious pathogens, saving blood banks time and costs required for analysis of mandatory pathogens. The IVD test is a multiplex immunoassay that simultaneously screens for six bloodborne infectious diseases per blood sample. In this project, a mix of diagnostic protein markers will be developed and validated to lowdown an IVD test ready for commercial scale-up and CE-IVD certification.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date December 30, 2023
Est. primary completion date December 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria: - Samples having been tested positive or negative for the serological markers explored in the study Exclusion criteria: - to refuse to participate to the study

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Uhmontpellier Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Analytical performances Analytical performances day 1
Secondary Number of Field evaluation Field evaluation day 1
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