MedPath

Study on Fluids Associated to Lung Cancer

Not Applicable
Completed
Conditions
Lung Cancer
Registration Number
NCT02853006
Lead Sponsor
University Hospital, Grenoble
Brief Summary

The diagnosis of lung cancer is the first cause of cancer deaths for man and woman. It requires invasive procedures (at least endoscopy, transthoracic puncture, or surgery).

This study is about the set up of an innovative test for lung cancer prognosis, based on biopsies and surgical material : LungCancerTest, with the creation of a start-up in progress.

The main goal of this study is to approve the diagnostic value of the molecular signature of the 26 genes (LungCancerTest) revealed in blood and respiratory fluids among patients with lung cancer.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
31
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Quantification of : DNAHalf a day

From plasma or respiratory fluids, with Qiagen QIAamp MinElute Virus Spin kit.

Picogreen technique (fluorimétrie) with the device Qubit 2.0 Characterization of DNA by migration on revealed agarose gel in presence of ethidium bromide

Study of DNA (mutation, reassortment) with New Generation Sequencing materiel.

Quantification of : RNAHalf a day

From plasma or respiratory fluids, with Qiagen QIAamp MinElute Virus Spin kit.

Picogreen technique (fluorimétrie) with the device Qubit 2.0 Characterization of RNA with an Agilent chip

Study of RNA (LungCancerTest) with PCR-Array prototype to show the expression of the molecular signature (Cancer Testis genes).

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

UniversityHospitalGrenoble

🇫🇷

La Tronche, France

UniversityHospitalGrenoble
🇫🇷La Tronche, France

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.