Skip to content

Prospective open label randomized controlled study on the treatment of pure ground glass nodules in the lungs with Jinju formula

Prospective open label randomized controlled study on the treatment of pure ground glass nodules in the lungs with Jinju formula

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000252
Enrollment
Unknown
Registered
2025-02-13
Start date
2024-11-01
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Pulmonary nodule

Interventions

Control group:Clinical observation

Sponsors

The First Affiliated Hospital of Naval Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients who meet all of the following criteria within 21 days prior to screening observation will be included in the study: (1) Gender not limited age between 18-80 years old; (2) The first discovery of pulmonary nodules within 3 months can provide chest CT examination results indicating: 5mm < pure ground glass nodules = 10mm; Single or multiple if multiple with no more than 10 pulmonary nodules and evaluated based on the largest nodule; (3) The nodules have remained stable without growth or dissipation within the past three months; (4) Voluntarily participate in the experiment and sign the informed consent form.

Exclusion criteria

Exclusion criteria: Patients who meet one of the following criteria within 21 days prior to screening and observation will be excluded from the study: (1) Patients with other primary malignant tumors; (2) Diagnosed with pulmonary tuberculosis pulmonary fungal disease pneumonia or other lung diseases with clear causes currently may require Those who need to undergo immediate anti tuberculosis anti fungal anti infection or other related treatments; (3) Lung CT can directly observe malignant signs such as spicules lobulation vascular bundle shadows vacuoles pleural traction and increased solid components in non solid nodules; (4) Diagnosis of spleen kidney yang deficiency based on traditional Chinese medicine syndromes; (5) Individuals with serious illnesses or functional disorders of the heart liver kidneys etc; (6) Pregnant or lactating women; (7) Individuals with mental or cognitive impairments; (8) Participants in other drug trials; (9) Individuals who are allergic to the drugs used in this study.

Design outcomes

Primary

MeasureTime frame
Total efficiency;

Secondary

MeasureTime frame
Changes in tumor markers compared to baseline;Risk score determination for malignant transformation;Evaluation of Traditional Chinese Medicine Syndrome Efficacy;

Countries

China

Contacts

Public ContactZhai Xiaofeng

The First Affiliated Hospital of Naval Medical University

zhaixfch@163.com13917595511

Outcome results

None listed

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