Skip to content

Effects of Qizhen capsule on the prevention of recurrence and metastasis of non-small cell lung cancer after surgery: a multicenter randomized controlled clinical trial

Effects of Qizhen capsule on the prevention of recurrence and metastasis of non-small cell lung cancer after surgery: a multicenter randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001420
Enrollment
Unknown
Registered
2025-07-16
Start date
2025-09-01
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

Control group:Placebo + standard chemotherapy regimen after surgery for non-small cell lung cancer
Experimental group:Qizhen capsule + standard chemotherapy regimen after surgery for non-small cell lung cancer

Sponsors

Beijing Hospital of Traditional Chinese Medicine Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Patients after radical surgery for stage Ib-III non-small cell lung cancer (2) Mutations in driver genes such as EGFR/ALK are negative or unknown (3) The first adjuvant chemotherapy is planned to be performed within 6 weeks after surgery (4) ECOG score 0-2 points (5) Aged 18-75 years old the bone marrow and important organ functions meet chemotherapy requirements (6) Good compliance and sign an informed consent letter

Exclusion criteria

Exclusion criteria: (1) Patients without clear pathological diagnosis (2) Patients with recurrence and metastasis before the first adjuvant treatment (3) Patients suffering from other primary malignant tumors at the same time (4) Pregnant and breastfeeding women or those with serious diseases of the heart lung liver kidney blood etc. the researchers believe that it is not suitable for enrollment. (5) Patients who are known to be allergic to research medication (6) Patients undergoing other drug trials

Design outcomes

Primary

MeasureTime frame
2-year Disease-Free Survival rate;

Secondary

MeasureTime frame
1-Year/2-Year Overall Survival Rate(1-year/2-year OS rate);Median Overall Survival(mOS);Chemotherapy adverse reactions;Median Disease - Free Survival(mDFS);T lymphocyte subsets and cytokines;quality of life;1-Year Disease-Free Survival Rate;syndromes\tongue and pulse conditions\symptoms of Traditional Chinese Medicine;

Countries

China

Contacts

Public ContactXiaomin Wang

Beijing Hospital of Traditional Chinese Medicine Capital Medical University

ntxm100@sina.com13051272736

Outcome results

None listed

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