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Translational results of combining chemotherapy with Jinshui Liujun Decoction for EGFR wild-type non-small cell lung cancer

Translational results of combining chemotherapy with Jinshui Liujun Decoction for EGFR wild-type non-small cell lung cancer

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061484
Enrollment
Unknown
Registered
2022-06-26
Start date
2022-06-13
Completion date
Unknown
Last updated
2023-04-03

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 (NSCLC)

Interventions

Experimental group:Chemotherapy combined with the addition of Jin Shui Liu Jun Decoction
Control group:Chemotherapy

Sponsors

The First Affiliated Hospital of Hebei North University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 78 Years

Inclusion criteria

Inclusion criteria: 1. The patient was diagnosed with Stage III to IV non-small cell lung cancer by pathology or cytology and was diagnosed with EGFR wild type by genetic test; 2. Karnofaky score >=60, predicted survival of more than 3 months; 3. Patients unable or unwilling to undergo surgery; 4. Aged <=78 years; 5. All examination indicators are in line with indications of chemotherapy; 6. Patients with observable tumor foci, willing to accept the treatment program, able to adhere to medication according to the doctor's advice, good compliance, patients can be followed up, TCM syndrome differentiation is Qi and Yin deficiency, heat stasis internal resistance.

Exclusion criteria

Exclusion criteria: 1. Those with cognitive impairment who cannot cooperate well or limited education level who cannot understand and fill in the form; 2. Failure of heart, lung, liver, kidney and other major organs; 3. Patients who are allergic to drugs used in this study; 4. Mental and neurological disorders, unable to express their wishes correctly; 5. Pregnant patients, lactating patients and patients of childbearing age who do not take contraceptive measures; 6. Patients currently participating in clinical trials of other drugs or medical devices.

Design outcomes

Primary

MeasureTime frame
Disease control rate;Objective response rate (ORR);

Secondary

MeasureTime frame
TCM evidence score;Karnofaky score;Immune cytokines;

Countries

China

Contacts

Public ContactLiu Daiwei

The First Affiliated Hospital of Hebei North University

chequan1225@126.com+86 15530391323

Outcome results

None listed

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