Differentiating Benign and Malignant Pulmonary Nodules Using Epigenetically Modified Nucleosomes in Plasma

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

We aim to evaluate the diagnostic accuracy of the Nu.Q blood test for lung cancer in the Taiwanese population and compare its diagnostic performance with low-dose computed tomography (LDCT) or computed tomography (CT). Additionally, we will investigate the potential role of Nu.Q in lung cancer prevention and its impact on survival outcomes. Study Method: We plan to collect 20 mL of blood samples from individuals undergoing chest LDCT/CT, isolate plasma for Nu.Q™ analysis, and compare the results with corresponding lung cancer pathology findings. The estimated sample size is 500 participants.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 20
Healthy Volunteers: f
View:

• Aged 20 or older

• Underwent a low-dose chest CT scan or a standard chest CT scan, showing lung nodules ≥ 6mm

• Individuals understand the content of the consent form and are willing to participate in this study.

• The lung nodule is assessed by a physician as high-risk, requiring thoracic surgery or biopsy for diagnosis

Locations
Other Locations
Taiwan
National Taiwan University
RECRUITING
Taipei
Contact Information
Primary
Pei-Hsing Chen, MD
chenph@ntu.edu.tw
886-2-2312-3456 Ext. 53422
Backup
Jin-Shing Chen, M.D., Ph.D.
chenjs@ntu.edu.tw
86-2-2322-0322
Time Frame
Start Date: 2025-03-11
Estimated Completion Date: 2026-02-28
Participants
Target number of participants: 500
Related Therapeutic Areas
Sponsors
Collaborators: Volition Diagnostics UK Ltd
Leads: National Taiwan University Hospital

This content was sourced from clinicaltrials.gov