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Clinical Study on Shuanghuang Yangxue Decoction in Treating Patients with Lung Cancer Related Anemia and Serum Iron Deficiency

Analysis of Related Factors of Lung Cancer Related Anemia and Clinical Study of Shuanghuang Yangxue Decoction on Patients with Serum Iron Deficiency

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077699
Enrollment
Unknown
Registered
2023-11-16
Start date
2023-11-30
Completion date
Unknown
Last updated
2023-11-21

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

Conditions

Lung Cancer Related Anemia and Serum Iron Deficiency

Interventions

control group:Ferrous succinate
Treatment group:Ferrous succinate and Shuanghuang Yangxue Decoction

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Patients with lung cancer diagnosed by pathology or cytology and meeting the diagnostic criteria for mild to moderate anemia: refer to the World Health Organization's anemia grading standard in the Clinical Practice Guide for Tumor related Anemia (2022 Edition) of the Chinese Society of Clinical Oncology (CSCO): Grade 0 (normal value): Hb of adult males is not less than 130g/L, Hb of non pregnant adult females is not less than 120g/L, and Hb of pregnant adult females is not less than 110g/L; Level 1 (mild): 110g/L~normal value; Grade 2 (moderate): 80g/L~109g/L; Grade 3 (severe):<80g/L; (2) Meet the standard of low serum iron level: according to the Standard for Diagnosis and Efficacy of Hematologic Diseases, serum iron<8.95 µ Mol/L is the standard of low serum iron level; (3) Those who have not received radiotherapy and chemotherapy in the past or have completed radiotherapy and chemotherapy for more than 1 month; (4) The TCM syndrome classification conforms to the patients with deficiency of both Qi and blood; (5) Patients who have not been treated with iron, EPO, blood transfusion, Qi tonifying and blood nourishing prescription or Chinese patent medicine 1 month before admission; (6) Cassegrain score = 60; (7) Age = 18 years old and = 80 years old, regardless of gender; (8) Those who voluntarily participate in this study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Acute blood loss or hemolysis; (2) Those who have participated in or are participating in other drug related clinical trials in the past month; (3) Those who are allergic to the study drug during treatment; (4) People with severe heart, liver, kidney and other organ dysfunction; (5) Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
Effective rate of anemia correction;

Secondary

MeasureTime frame
Blood routine examination;Indicators of anemia;Immunity index;Inflammatory cytokines;

Countries

China

Contacts

Public ContactJun Shi

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

shijundoctor@163.com+86 139 1731 1112

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 26, 2026