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Study for the effect of traditional Chinese medicine on the enhancement and attenuation of local advanced non-small cell lung cancer during radiotherapy and chemotherapy

Study for the effect of traditional Chinese medicine on the enhancement and attenuation of local advanced non-small cell lung cancer during radiotherapy and chemotherapy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2000003189
Enrollment
Unknown
Registered
2020-04-06
Start date
2020-05-01
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

Non-small cell lung cancer

Interventions

Sponsors

Shanghai Pulmonary Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients with locally advanced non-small cell lung cancer confirmed by pathology, who are not suitable for surgery and can accept radiotherapy and chemotherapy; 2. Patients aged 18-70 years old with ECoG PS 0-1 and expected survival time >=6 months; 3. For patients without major organ dysfunction and with basically normal heart, liver and kidney functions, the test indexes meet the following requirements: blood: leukocyte >4.0x10^9/L, neutrophil absolute value > 1.5x10^9/L, platelet count >100x10^9/L, hemoglobin >110g/L; liver function: serum bilirubin is 1.5 times lower than the maximum normal value; ALT and AST are 1.5 times lower than the maximum normal value; bun. Cr is within the normal range; 4. Pulmonary function: FEV1 >45%, DLCO >60% before treatment; 5. Patients without other cancers except stage I cervical cancer and skin basal cell carcinoma; 6. Patients with good compliance who can understand the situation of this study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with any acute or chronic diseases that are not suitable for radiotherapy and chemotherapy; 2. Patients with previous cancer history other than stage I cervical cancer and skin basal cell carcinoma, or who have undergone lobectomy or pneumonectomy; 3. Patients with active systemic infection or pulmonary or pericardial infection; 4. Pregnant or lactating women; 5. Patients with poor compliance with the protocol are not suitable for the study.

Design outcomes

Primary

MeasureTime frame
adverse effects;

Countries

China

Contacts

Public ContactYaping Xu

Shanghai Pulmonary Hospital?

xuyaping1207@163.com+86 21-65115006

Outcome results

None listed

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