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Therapy with FZQXF to prevent the relapse of postoperative patients with stage IB-IIB lung adenocarcinoma after surgery and adjuvant chemotherapy:a prospective, cohort, two-center clinical study

Therapy with FZQXF to prevent the relapse of postoperative patients with stage IB-IIB lung adenocarcinoma after surgery and adjuvant chemotherapy:a prospective, cohort, two-center clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000036042
Enrollment
Unknown
Registered
2020-08-21
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-08-31

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

Conditions

Stage IB-IIB lung adenocarcinoma

Interventions

Sponsors

Department of Oncology of Shanghai Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Patients conforming to lung adenocarcinoma, whose clinical stage was stage IB-IIB radical surgery and completed postoperative adjuvant therapy, and patients within 3 months after adjuvant chemotherapy; (2) Patients aged 18 to 80 years; (3) Blood routine and biochemical indexes are basically normal, and there is no serious virus or bacterial infection;Patients without organ failure or severe heart disease (hemobilirubin 3.5x10^9/L and lower than 12x10^9/L, platelet count>80x10^9/L, hematocrit >0.20); (4) No other serious complications; (5) I agree to participate in the study and sign the informed consent with good compliance. (6) Non-pregnant or lactating patients; (7) No allergic reaction to the compatible ingredients in the prescription.

Exclusion criteria

Exclusion criteria: (1) Patients with cancer recurrence or metastasis; (2) Patients receiving other drug intervention treatment (including other traditional Chinese medicine decoction pieces, chemotherapy, targeted drugs); (3) Having a mental illness; Lack of autonomous behavior ability; (4) Women who are pregnant or preparing for pregnancy or breastfeeding; (5) Patients with heart, lung, brain, liver, kidney, hematopoietic system and other serious diseases or mental diseases; (6) Allergic constitution or known allergy to the composition of this drug; (7) Patients who are participating in other clinical trials or who have participated in other clinical trials within 3 months; (8) Alcoholics and/or psychoactive substances, substance abusers and dependants; (9) According to the judgment of the researchers, there are other lesions or conditions that reduce the possibility of enrollment or complicate enrollment, such as frequent changes in the working environment and unstable living environment, which may easily lead to loss of follow-up.

Design outcomes

Primary

MeasureTime frame
PFS;OS;recurrence rate;

Secondary

MeasureTime frame
CEA;CY-211;NSE;SCC;NK cells (CD3-CD56dimCD16+);B cells (CD19+);T cell subsets (CD3+CD4+CD8+);Treg (CD4+CD25+Foxp3+);MDSC(CD11b+ Gr-1+);

Countries

China

Contacts

Public ContactLuo Yingbin

Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chin

dr.luo@qq.com+86 18801616061

Outcome results

None listed

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