Real-world Study on Shenbailing Granules for Improving Qi and Blood Deficiency in Patients After Breast Cancer Surgery
Launched by CAIGANG LIU · Mar 12, 2025
Trial Information
Current as of April 26, 2025
Enrolling by invitation
Keywords
ClinConnect Summary
This study plans to enroll patients who have undergone breast cancer surgery. The experimental group will receive Shenbailing granule therapy, with the primary objective of exploring the improvement of postoperative cancer-related fatigue and quality of life in breast cancer patients treated with Shenbailing granules. Patients will enter the real-world study phase immediately after surgery.
Experimental group: Adjuvant therapy with Shenbailing granules, starting from 1 day after surgery; Control group: Normal postoperative recovery without medication.
After confirming the surgery date, pa...
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- Subjects must meet all of the following enrollment criteria to be enrolled in this trial:
- • 1. be 18-75 years of age (both 18 and 75);
- • 2. female;
- • 3. all patients have histologically confirmed breast cancer;
- • 4. expected to receive surgical treatment;
- • 5. expected survival of ≥ 1 year;
- 6. the level of function of vital organs must meet the following requirements:
- • 1. Bone marrow function Absolute neutrophil count (ANC) ≥ 1.5 x 10\^9/L; Platelets ≥ 100 x 10\^9/L; Hemoglobin ≥ 90 g/L;
- • 2. Liver and kidney function Albumin level ≥ 3.0 g/dL; Total bilirubin ≤ 1.5 x upper limit of normal (ULN); Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5 × ULN; Alkaline phosphatase ≤ 2.5 x ULN; Urea nitrogen and serum creatinine ≤ 1.5 × ULN or creatinine clearance ≥ 60 mL/min (calculated according to the Cockcroft-Gault formula);
- • 3. Prothrombin time (PT) and activated partial thromboplastin time (APTT) ≤ 1.5 × ULN;
- • 4. Echocardiogram (ECHO) showing cardiac left ventricular ejection fraction (LVEF) ≥ 50%;
- • 8. voluntarily accept the treatment and sign the informed consent form, have understood the purpose of this study and the experimental steps, good compliance, and comply with the relevant requirements of this trial protocol.
- Exclusion Criteria:
- • 1. intolerance to or poor compliance with herbal medicines;
- • 2. inability to swallow, chronic diarrhea and intestinal obstruction, and the presence of multiple factors affecting the administration and absorption of medications;
- • 3. severe cardiac, hepatic, renal and other vital organ insufficiency;
- • 4. combination of serious complications, active infection, persistent fever, serious bleeding tendency, hematopoietic function abnormality;
- • 5. a known history of allergy to the drug components of this regimen;
- • 6. have a history of immunodeficiency, including testing positive for HIV, HCV, active viral hepatitis B, or suffering from other acquired, congenital immunodeficiency diseases, or have a history of organ transplantation
- • 7. a history of any cardiac disease, including (1) arrhythmia requiring medication or of clinical significance, (2) myocardial infarction, (3) heart failure, (4) any other cardiac disease judged by the investigator to be inappropriate for participation in the study, etc;
- • 8. pregnant or lactating female patients, female patients of childbearing potential with a positive baseline pregnancy test or female patients of childbearing potential who are unwilling to use effective contraception throughout the trial period;
- • 9. in the judgment of the investigator, have a serious concomitant medical condition that jeopardizes the patient's safety, or interferes with the patient's ability to complete the study (including, but not limited to, severe hypertension that cannot be controlled by medication, severe diabetes mellitus, active infection, etc.)
- • 10. is unconscious, non-verbal or non-reading, unable to communicate normally, and unable to cooperate in completing the questionnaire assessment;
- • 11. a previous history of a definite neurological or psychiatric disorder, including epilepsy or dementia
- • 12. suspected or confirmed history of alcohol or drug abuse;
- • 13. any other condition that, in the opinion of the investigator, makes the patient unsuitable for participation in this study.
About Caigang Liu
Caigang Liu is a dedicated clinical trial sponsor committed to advancing medical research and innovation. With a focus on ethical practices and patient safety, Liu oversees the design, implementation, and management of clinical trials across various therapeutic areas. Leveraging a strong background in clinical research and regulatory affairs, Liu ensures compliance with industry standards while fostering collaboration among stakeholders. Through a rigorous approach to data integrity and analysis, Caigang Liu aims to contribute meaningful insights that enhance treatment options and improve patient outcomes.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Shenyang, Chian/Liaoning, China
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported