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Clinical observation of auxiliary function of anti-inflammatory Chinese herbal medicine in chemotherapy of middle and advanced lung cancer

Clinical observation of auxiliary function of anti-inflammatory Chinese herbal medicine in chemotherapy of middle and advanced lung cancer

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050485
Enrollment
Unknown
Registered
2021-08-28
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

Lung cancer

Interventions

Sponsors

Hubei Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. The patients voluntarily joined the study, signed the informed consent form, and had good compliance. 2. Patients diagnosed with lung cancer according to imaging, cytology and histological examinations; patients diagnosed with lung cancer in stages IIIB-IV according to the 8th edition of the International Union Against Cancer (UICC) revised TNM staging. 3. Patients who are or will be receiving platinum-based chemotherapy. 4. Estimated survival > 3 months. 5. KPS score > 60 points. 6. Aged >= 18 years.

Exclusion criteria

Exclusion criteria: 1. Those with other active malignant tumors or those who have not recovered from other major operations before; 2. There are factors that obviously affect the absorption of oral drugs, such as inability to swallow, chronic diarrhea and intestinal obstruction; 3. Complicated with severe infection or confirmed to have other major physiological dysfunction; 4. Patients with serious diseases such as the heart, liver, kidney, hematopoietic system, as well as those with severe functional impairment, and mentally ill patients; 5. Pregnant and lactating patients; 6. Those who cannot cooperate with the treatment; 7. Allergic constitution, history of allergy to chrysanthemum, licorice, or history of severe food or drug allergy.

Design outcomes

Primary

MeasureTime frame
Quality of life;Chemotherapy-related adverse reactions;

Secondary

MeasureTime frame
Karnofsky score;Weight;

Countries

China

Contacts

Public ContactWang Jun

Hubei Cancer Hospital

670706100@qq.com+86 13469996007

Outcome results

None listed

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