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A multicenter randomized controlled trial to assess the efficacy of cancer green therapy in treatment of stage IIIb/IV non-small cell lung cancer

A multicenter randomized controlled trial to assess the efficacy of cancer green therapy in treatment of stage IIIb/IV non-small cell lung cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR1900002748
Enrollment
Unknown
Registered
2019-11-13
Start date
2020-01-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

lung cancer

Interventions

Sponsors

Dongfang Hospital Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Patients with histologically or cytologically confirmed NSCLC, and clinical stage IIIb or IV. (2) One of above five TCM syndrome pattern differentiation; (3) There is at least one lesion larger than 2cm in diameter that can be cryoablation in the lung; (4) The Eastern Cooperative Oncology Group (ECOG) score <= 2 and the expected survival time was more than 3 months (5) Aged more than 18 years; (6) Able to read Chinese and willingness to provide signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients who had received any radiation, chemotherapy, targeted therapy or immunotherapy for their cancers within a month; (2) Patients with symptomatic brain metastases; (3) Patients with infectious and radioactive inflammation around the lesion, or skin infection and ulceration at the puncture site; (4) Patients with severe pulmonary fibrosis especially drug-induced pulmonary fibrosis; (5) Patients with severe bleeding tendency, platelet less than 50×109/L and severe coagulation disorders; (6) Patients with poor control of ipsilateral malignant pleural effusion; (7) Pregnant and lactating women; or severe insufficiency of liver, kidney, heart, lung and brain; or severe anemia, dehydration and serious disorders of nutrition metabolism, unable to be corrected or improved in a short time; or patients with severe systemic infection and high fever (T > 38.5 degree C). (8) HIV antibody positive or with other acquired or congenital immunodeficiency diseases; (9) Patients with a history of organ transplantation; (10) Patients enrolled in other clinical trials within three months.

Design outcomes

Primary

MeasureTime frame
overall survival time;

Countries

China

Contacts

Public ContactKaiwen Hu
kaiwenh@163.com+86 13911650713

Outcome results

None listed

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