Skip to content

The MDA Test to Differentiate of Benign and Malignant Pulmonary Nodules

Targeted Chromosomal Aberrations Detection by FISH Analysis of Circulating Abnormal Cells to Differentiate of Benign and Malignant Pulmonary Nodules

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03790735
Enrollment
200
Registered
2019-01-02
Start date
2018-05-03
Completion date
2019-06-30
Last updated
2019-01-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulmonary Nodule, Solitary

Keywords

pulmonary nodule

Brief summary

* The purpose of the study is the identification of the efficacy of MDA Test to Differentiate of Benign and Malignant Pulmonary Nodules. * In this study, the investigators are going to validate the efficacy of the MDA test for diagnosing early lung cancer by comparing results of the pre-surgery MDA test with the post-surgery pathology.

Detailed description

* Current state-of-the-art lung cancer early screening utilizes low-dose CT scan to identify lung nodules smaller than 3 cm in diameter. However, it's still a clinical challenge to differentiate between malignant and benign nodules. * This study is being conducted to evaluate the efficacy of the MDA TEST to detect Targeted chromosomal aberrations in circulating abnormal cells by FISH analysis that might be an early indicator of lung cancer. Approximately 200 Pre-surgery adult patients with single pulmonary nodule found by CT scan, will be enrolled in the study. The sample type of MDA test is Peripheral Blood. This study will compare the results of the pre-surgery MDA Test with the post-surgery pathology to determine if the test can detect lung cancer or the lack of lung cancer . * The results of the test will not be provided to the subject, the investigator and will not be used to diagnose or treat the subject.

Interventions

DIAGNOSTIC_TESTFISH

Targeted chromosomal aberrations detection

Sponsors

Zhuhai livzon cynvenio diagnostics LTD
CollaboratorUNKNOWN
Tianjin Medical University Cancer Institute and Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 18 years old or above * single pulmonary nodule found by CT scan. * the diameter of the pulmonary nodule is between 5mm to 30mm. * plan to accept pneumonectomy due to the pulmonary nodule. * agree to sign informed consent

Exclusion criteria

* fail to understand or agree to sign informed consent. * pregnant or lactating women. * the diameter of the pulmonary nodule is more than 30mm. * there are 2 or more pulmonary nodules in one single patient.

Design outcomes

Primary

MeasureTime frameDescription
Early detection of lung cancer6 monthsThe efficacy of the MDA TEST assay comparing with pathologic diagnosis(the gold standard), and CT/LDCT diagnosis, including sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV).

Countries

China

Contacts

Primary ContactDongyan Cheng
chengdongyan916@163.com(022)23340123-6012

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026