Cancer-related Fatigue in Patients With Breast Cancer Treatment With Zhengyuan Capsules

Официальное название

A Multi-center, Randomized, Double-blind, Placebo-controlled Clinical Study on the Effectiveness and Safety of Zhengyuan Capsules for Cancer-related Fatigue in Patients With Breast Cancer

Обзор

Traditional Chinese medicine（TCM） has achieved some meaningful results in improving the symptoms and quality of life of cancer patients, but many research results need to be further verified by clinical trials with larger samples and better design.This study aims to investigate effectiveness and safety of Zhengyuan Capsules for cancer-related fatigue in patients with breast cancer.

Подробное описание

By conducting multi-center, randomized, double-blind, placebo-controlled clinical research to investigate effectiveness and safety of Zhengyuan Capsules for cancer-related fatigue in patients with breast cancer.This test choose the improvement of fatigue degree as key indicator, and choose the improvement both symptoms of patients and quality of life as second indicators. And last, the study will try to verify its safety and efficacy with some haematological indexs and reveal its mechanism from the perspectives of Cytokines and immunological indicators, so as to explore the advantages of traditional Chinese medicine（TCM） in the treatment of CRF and support some high quality, internationally recognized clinical evidence.

Вмешательства

• Препарат Zhengyuan Capsules
  Zhengyuan capsules, 4 capsules at a time, 3 times per day;
• Препарат Placebo contains 5%-10% Zhengyuan Capsule total mixed powder
  Zhengyuan capsules simulator（Placebo contains 5%-10% Zhengyuan Capsule total mixed powder）, 4 capsules at a time, 3 times per day;

Первичные конечные точки

• Fatigue degree with the Brief Fatigue Inventory（BFI） [Срок оценки: 8 weeks]

Вторичные конечные точки (4)

• Fatigue degree the Revised Piper Fatigue Scale（PFS⁃R） [Срок оценки: 8 weeks]
• Fatigue degree with the MD Anderson Symptom Inventory（MDASI） [Срок оценки: 8 weeks]
• Change of patients' functional status with Karnofsky performance status (KPS) [Срок оценки: 8 weeks]
• Quality of Life Questionnaire-Breast Cancer Module 23（QLQ-BR23） [Срок оценки: 8 weeks]

Критерии участия

Критерии включения

• Histopathologically or cytologically confirmed as breast cancer; AJCC 8th edition staging for breast cancer is stages I to III, clinically and radiologically confirmed with no tumor recurrence or metastasis.
• Completed anti-tumor treatment (surgery, radiotherapy, chemotherapy, targeted therapy) for at least 2 months, with no planned anti-tumor treatment during the study period, excluding endocrine therapy.
• Meets the diagnosis criteria for cancer-related fatigue.
• Average score on the Brief Fatigue Inventory (BFI) in the 14 days preceding enrollment is ≥4.
• Life expectancy of at least 6 months.
• Age between 18 and 70 years old.
• Patients and their families understand the basic details of the study, agree to cooperate in completing the relevant research; the patient can communicate verbally and in writing; voluntary signing of the informed consent form.

Критерии исключения

• Presence of significant liver or kidney dysfunction (e.g., alanine transaminase, aspartate transaminase greater than 3 times the upper limit of normal, blood creatinine greater than 1.5 times the upper limit of normal, eGFR \<60 mL/min/1.73m²) or abnormalities in the hematological system (platelet count \<75×10⁹/L, hemoglobin \<100g/L, or neutrophil count \<1.5×10⁹/L);
• Presence of severe primary diseases in the cardiovascular, cerebrovascular, immune systems, or requiring treatment for mental illness;
• Hypokalemia (blood potassium \<3.0mmol/L) or electrolyte imbalance with related symptoms or symptoms that may occur after enrollment;
• Unimproved hypothyroidism;
• Hypoalbuminemia (blood albumin \<30g/L) or malnutrition (Body Mass Index, BMI \<18 kg/m²);
• Traditional Chinese medicine syndrome pattern consistent with Yin deficiency and internal heat;
• Use of medications indicated in the instructions or with main functions that meet the following conditions: other Western or Chinese medicine preparations that affect the efficacy evaluation of cancer-related fatigue; undergoing treatment with anti-anemia, anti-anxiety/depression, anti-insomnia, or other psychostimulant drugs; use of drugs with leukocyte-increasing effects within the past week, such as granulocyte colony-stimulating factor (G-CSF);
• Known allergy to the investigational drug or its components;
• Breastfeeding, pregnant, or planning to become pregnant within 3 months;
• The investigator deems the individual unsuitable for participation in this clinical trial.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Рандомизированное

Модель

Параллельные группы

Маскирование

Четверное слепое

Основная цель

Поддерживающая терапия

Центры проведения

Список центров уточняется — проверьте первичный протокол.

Идентификаторы

NCT: NCT06381557 · YRPG-PMS-ZYJN-RCT-2022-01

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗