Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06097156

Evaluation of See.d as an Automated Blood Sample Preparator for Multiple Liquid Biopsy Applications

Feasibility Evaluation of See.d Pre-Analytical Platform Performance: From Whole Blood to Plasma and SBS Slides for Liquid Biopsy Applications

Status
Recruiting
Phase
Study type
Observational
Enrollment
45 (estimated)
Sponsor
Tethis S.p.A. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

This study aims to evaluate the feasibility of using See.d instrument and SBS slides for preparation of plasma and cytological samples from whole blood. Forty-five participants will be enrolled (20 healthy volunteers and 25 metastatic breast cancer patients) and each participant will be asked to provide a blood sample.

Detailed description

The goal of this study is the evaluation of a new instrument called See.d, to be used in conjunction with its accessories, Smart Bio Surface (SBS) slides, for preparation of cytological samples (seeded on SBS slides) and plasma from fresh whole blood (within 4-6 hours from collection). Blood samples collected from healthy volunteers will be spiked-in with reference DNA and mock-CTC to mimic a patient sample in order to evaluate the instrument performance through the analysis of several parameters. Blood samples from Metastatic Breast Cancer (MBC) patients will be processed with See.d instrument installed in a clinical context to perform a preliminary analytical characterization of either cell-free DNA (cfDNA) and Circulating Tumor Cells (CTC). For its feasibility nature, no formal statistics has been planned for this study.

Conditions

Timeline

Start date
2023-11-06
Primary completion
2026-12-01
Completion
2026-12-01
First posted
2023-10-24
Last updated
2026-01-30

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT06097156. Inclusion in this directory is not an endorsement.