Clinical Trials Directory

Trials / Completed

CompletedNCT05546632

Evaluation of Cyto-chex Tubes for the Measurement of Monocyte Expression of Human Leukocyte Antigen - DR Isotype (HLA-DR) Molecules by Flow Cytometry

Evaluation of Cyto-chex Tubes for the Measurement of Monocyte Expression of HLA-DR Molecules by Flow Cytometry

Status
Completed
Phase
Study type
Observational
Enrollment
40 (actual)
Sponsor
Hospices Civils de Lyon · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The expression of mHLA-DR, measured by flow cytometry, is today the reference marker to guide immunostimulatory therapies (IFN-γ) in the most severely immunocompromised patients. Nevertheless, pre-analytical constraints (storage of samples at +4°C before analysis) limit the wide use of mHLA-DR in clinical practice (problem of transporting samples to sites with a flow cytometer). Recent studies have shown that samples taken on Cyto-Chex Blood Collection Tubes (BCT) (containing a cell membrane stabilizer) were, for mHLA-DR, stable at room temperature during 72 hours after sampling. The main objective of this study is to compare the expression of mHLA-DR from samples taken simultaneously from standard tubes (EDTA) and new generation Cyto-Chex BCT tubes, to validate using Cyto Chex BCT tube in the clinical practice. The investigators think that mHLA-DR quantification performed from Cyto-Chex BCT tubes is reliable and similar to quantification performed from EDTA tubes.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTBlood samplingPatients will have one blood sampling using one EDTA tube and one Cyto-Chex BCT tube, one after the other

Timeline

Start date
2022-10-13
Primary completion
2022-11-14
Completion
2022-11-14
First posted
2022-09-21
Last updated
2024-06-12

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT05546632. Inclusion in this directory is not an endorsement.