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Clinical study of Buzhongyiqi granule in the treatment of lung cancer related fatigue with deficiency of lung-spleen qi

Clinical study of Buzhongyiqi granule in the treatment of lung cancer related fatigue with deficiency of lung-spleen qi

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057219
Enrollment
Unknown
Registered
2022-03-04
Start date
2022-03-01
Completion date
Unknown
Last updated
2023-10-09

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

Conditions

Cancer-related fatigue

Interventions

treatment group:Symptomatic treatment and Buzhong Yiqi granule
control group:Symptomatic treatment

Sponsors

Renmin Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Non-small cell lung cancer patients who met the Western diagnostic criteria for primary lung cancer and TNM stage ?-?, regardless of metastasis (refer to the Western diagnostic criteria for non-small cell lung cancer formulated by the Chinese Standard for the Diagnosis and Treatment of Primary Lung Cancer (2018 edition) and the eighth edition TNM staging of lung cancer formulated by the International Association for the Study of Lung Cancer (IASLC) in 2017); 2. Meeting the diagnostic criteria for cancer-related fatigue (CRF) (referring to the CRF diagnostic criteria proposed in the tenth Revision of the International Classification of Diseases (ICD-10)); 3. TCM syndrome was diagnosed as lung qi deficiency syndrome (refer to the lung cancer diagnosis and treatment plan of the National Administration of Traditional Chinese Medicine 11th Five-Year Plan Key Specialist Collaboration Group); 4. The estimated survival time is greater than 6 months; 5. KPS functional status score is greater than 60; 6. Aged between 18 and 80 years; 7. Willing to accept the treatment of this protocol, with good compliance and signed informed consent; 8. Those who have completed all antitumor therapy or are undergoing antitumor therapy are currently in the interval of antitumor therapy, and the interval period is longer than 30 days, which is sufficient to complete the treatment of this protocol.

Exclusion criteria

Exclusion criteria: 1. Those with mental illness who cannot complete the rating scale; 2. Allergic to clinical research drugs; 3. Pregnant or lactating patients; 4. Patients with severe hypertension, heart, liver, kidney, blood system diseases and complications; 5. Taking traditional Chinese medicine or proprietary Chinese medicine containing Buzhong Yiqi Granule.

Design outcomes

Primary

MeasureTime frame
Functional Assessment of Chronic Illness Therapy-Fatigue;

Secondary

MeasureTime frame
The Fatigue Symptom Inventory;Symptom Inwentory for TCM;Karnofsky Performance Score;Inflammatory factor;

Countries

China

Contacts

Public ContactMei Shasha

Renmin Hospital of Wuhan University

13554496981@126.com+86 18986284493

Outcome results

None listed

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