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A randomized controlled study of YiQi YangYin prescription combined with chemotherapy and bevacizumab in post-secondary treatment of NSCLC

A randomized controlled study of Yiqi Yangyin prescription combined with chemotherapy and bevacizumab in post-secondary treatment of NSCLC

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000440
Enrollment
Unknown
Registered
2025-02-28
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Lung cancer

Interventions

treatment group:YiQi YangYin prescription+Chemotherapy + Angiogenesis inhibitor ± PD-1 inhibitor
Control group:Chemotherapy + Angiogenesis inhibitor ± PD-1 inhibitor

Sponsors

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Age =18 years old and =75 years old gender is not limited; (2) Patients with pathologically or cytologically confirmed non-small cell lung cancer; (3) TNM stage III-IV with evaluable target lesions; (4) Chemotherapy combined with bevacizumab combined or non-combined immunotherapy should be used for second-line and above; (5) TCM syndrome type is Qi-Yin deficiency type patients; (6) PS (physical condition score) score < 3 expected survival =3 months.

Exclusion criteria

Exclusion criteria: (1) Serious uncontrolled organic disease or infection; (2) Active bleeding or arterial thromboembolism or gastrointestinal perforation; (3) Urinary protein greater than 2g/24h or abnormal blood routine liver and kidney function more than 3 degrees or stool occult blood more than 3+; (4) Patients who have received major surgery within one month; (5) Patients unable to eat; (6) Those who are unable to fill in the scale due to the disorder of consciousness and literacy; (7) Patients with a history of uncontrollable mental illness; (8) People who are allergic to Chinese medicine ingredients in this study; (9) Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Objective Response Rate;

Secondary

MeasureTime frame
;Disease Control Rate;Progression-Free-Survival;Hematological Testing;

Countries

China

Contacts

Public ContactXuanting Ye

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine Shanghai University of Traditional Chinese Medicine

yxting1231@163.com15921475329

Outcome results

None listed

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