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Fuzheng Kang’ai decoction in the treatment of cancer-related fatigue on advanced non-small cell lung cancer patients: A randomized controlled study

Fuzheng Kang’ai decoction in the treatment of cancer-related fatigue on advanced non-small cell lung cancer patients: A randomized controlled study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016547
Enrollment
Unknown
Registered
2018-06-07
Start date
2018-06-10
Completion date
Unknown
Last updated
2018-06-11

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

control group:chemotherapy plus placebo granules
treatment group:chemotherapy plus FZKA granules

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. confirmed advanced NSCLC (stage IIIB or IV) with histologic features of adenocarcinoma,squamous cell carcinoma or adenosquamous carcinoma; 2. Aged 18 to 80 years old; 3. Chemotherapy patients receiving chemotherapy of any platinum; 4. Performance status score of Eastern Cooperative Oncology Group (ECOG) is 0 to 2; 5. Measurable lesions in accordance with the Response Evaluation Criteria in Solid Tumors (RECIST); 6. Proper function in bone, liver, kidney, heart and lung; 7. Good patients compliance and sign the informed consent paper.

Exclusion criteria

Exclusion criteria: 1. Expected life expectancy of less than three months; 2. Diagnosed with brain metastasis that has not been in well controlled; 3. Pericardial effusion or ascites necessitating drainage; 4. Active double cancer; 5. Pregnant or breastfeeding at present.

Design outcomes

Primary

MeasureTime frame
FACIT-F;

Secondary

MeasureTime frame
EORTC QLQ-C30;

Countries

China

Contacts

Public ContactWanyin Wu

Guangdong Provincial Hospital of Chinese Medicine

wwanyin@126.com+86 13078869078

Outcome results

None listed

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