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Combined CT and exosomal diagnosis of early lung cancer

Combined CT and exosomal diagnosis of early lung cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800016303
Enrollment
Unknown
Registered
2018-05-24
Start date
2018-06-01
Completion date
Unknown
Last updated
2018-05-28

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

Conditions

Early lung cancer

Interventions

Gold Standard:Pathological diagnosis
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Sponsors

The Second Affiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Aged18 years male or female; 2) No acute severe disease; 3) Pulmonary nodules found on chest radiographs or LDCT examinations and disseminated pulmonary tuberculosis (diameter: 5mm=nodules=3cm). There are microscopic examinations, biopsy or indications for surgery (need to follow-up Pathological diagnosis results); 4) Patients with previously diagnosed lung nodules have not been diagnosed; 5) No history of surgical treatment of the lungs; 6) Patients who have not received targeted drugs, biological treatments, immunosuppressants, and modulators; 7) No organ transplant; 8) Written written informed consent and compliance with study protocol before willingness to conduct clinical research

Exclusion criteria

Exclusion criteria: 1) Pulmonary nodules have undergone surgical treatment; (considering that surgery has been performed, there is interference with the study); 2) history of organ transplantation such as lung transplantation; (consider the use of allogeneic genes and immunosuppressive agents); 3) Pregnancy or lactation; (Considering the inability to perform regular CT follow-up and the effects of fetal components); 4) HIV-positive or AIDS-related disease is known only; (taking into account interference with the use of immune drugs); 5) are receiving targeted drugs, immunosuppressive agents, immunomodulators, biological therapy patients; 6) Pulmonary tuberculosis during active period (consider infectious and referral loss factors); 7) RNA-like viral infections such as SARS, HIV, hepatitis virus (except for hepatitis B, other four Species are RNA viruses), influenza virus, bird flu virus, H5N1, Ebola, hemp Rash; 8) Various hematological diseases such as leukemia, lymphoma, aplastic anemia, MDS, Other types of anemia, hemolysis, hemophilia, DIC, etc.; 9) The history of blood transfusion (within 3 to 6 years) and the potential for blood transfusion; 10) Patients with neurological and mental diseases that cannot be matched; 11) Emergency treatment for acute and severe diseases; 12) Written written informed consent and compliance with study protocol before reluctant to conduct clinical studies.

Design outcomes

Primary

MeasureTime frame
pathology;The amount of deliberate exosomes in the peripheral blood;The amount of specific exosomes in cancerous tissue;The amount of specific exosomes in adjacent tissues;

Countries

China

Contacts

Public ContactGong Jianping

The Second Affiliated Hospital of Soochow University

gongjianpingsz@126.com+86 13701415049

Outcome results

None listed

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