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Clinical and Metabolomic Studies on the Treatment of Advanced Non-small Cell Lung Cancer with agreed Prescription Sanchong Tongluo Sanjie Capsules Combined with Conventional Regimen

Clinical and Metabolomic Studies on the Treatment of Advanced Non-small Cell Lung Cancer with agreed Prescription Sanchong Tongluo Sanjie Capsules Combined with Conventional Regimen

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001386
Enrollment
Unknown
Registered
2025-07-11
Start date
2025-07-17
Completion date
Unknown
Last updated
2025-07-21

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

Experimental group:Orally take the agreed - upon prescription Sanchong Tongluo Sanjie CapsulesConventional Western anti - cancer treatment Conventional traditional Chinese medicine treatment
control group:Conventional Western anti - cancer treatment , Conventional traditional Chinese medicine treatment

Sponsors

Shenzhen Bao'an Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1: treated patients with stage IV NSCLC who meet the diagnostic criteria. 2: Patients aged between 20 and 80 years old. 3: Patients with an estimated survival period of more than 3 months 4: Patients with a Karnofsky Performance Status (KPS) score of = 60 points. 5: Patients or their agents are able to read understand and fill out relevant forms

Exclusion criteria

Exclusion criteria: 1: The pathological diagnosis is unclear. 2: Patients who have other malignancies concurrently. 3: Patients with severe underlying diseases such as those with liver or kidney failure who cannot tolerate the treatment. 4: Pregnant or lactating women and patients with mental illnesses 5: Patients who are allergic to the study drugs. 6: Patients who are currently participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Short-term curative effect;

Secondary

MeasureTime frame
Squamous Cell Carcinoma Antigen;Plasma D-dimer;Traditional Chinese Medicine symptom score and therapeutic effect;Cytokeratin 19 Fragment(CYFRA21-1);Neuron-Specific Enolase;Carcinoembryonic Antigen(CEA);Metabolomics;

Countries

China

Contacts

Public ContactLIYang

Shenzhen Bao'an Traditional Chinese Medicine Hospital

liyang2001@126.com15814420030

Outcome results

None listed

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