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A clinical study on the identification of diagnostic biomarkers for lung cancer using high-throughput serum proteomics

A clinical study on the identification of diagnostic biomarkers for lung cancer using high-throughput serum proteomics

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400090572
Enrollment
Unknown
Registered
2024-10-08
Start date
2024-10-08
Completion date
Unknown
Last updated
2024-10-15

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

Conditions

Lung cancer

Interventions

Index test:Analysis results of serum proteomics testing

Sponsors

Zhejiang cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Common inclusion criteria (both groups of people must meet all of the following criteria): (1) Age = 18 years old; (2) Through chest CT examination, pulmonary nodules with a diameter of = 30mm were found; (3) Having complete clinical information; (4) Understand the research and have the willingness to sign an informed consent form; Individual inclusion criteria: Malignant pulmonary nodule group: Imaging suggests that the nodule may be highly malignant, and subsequent surgery or biopsy pathology confirms it as primary lung cancer. Benign pulmonary nodules group: those who are considered to have a high possibility of benign conditions based on imaging examinations and clinical manifestations, and therefore adopt conservative treatment strategies; Or if the imaging suggests malignancy, but it is confirmed by pathology to be a benign nodule.

Exclusion criteria

Exclusion criteria: (1) Individuals with a history of primary lung cancer or other malignant tumors (including multiple myeloma, monoclonal immunoglobulin disease, and other cancers that cause excessive serum immunoglobulin levels); Received anti-tumor treatment before enrollment, including surgical treatment, radiotherapy, chemotherapy, etc; (2) Individuals who have undergone lung resection or percutaneous lung biopsy prior to enrollment; (3) Blood transfusion recipients within 30 days prior to enrollment; (4) Pregnant or lactating women; (5) Other researchers believe that it is not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Proteomics;Accuracy;Sensitivity;Specificity;

Secondary

MeasureTime frame
Positive predicative value;Negative predictive value;

Countries

China

Contacts

Public ContactJian Zeng

Zhejiang cancer hospital

hzzengjian123@163.com+86 571 8812 8161

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026