jRCTs031220576招募中不适用
An open-label, randomized, controlled study of Ninjinyoeito for nontuberculous mycobacterial pulmonary disease with weight loss and anorexia (NYT for NTM-PD with weight loss and anorexia)
未提供0 个研究点目标入组 50 人开始时间: 2023年8月30日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 50
- 主要终点
- -
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized Controlled Trial
- 干预模型
- Parallel Assignment
- 主要目的
- Treatment Purpose
- 盲法
- Open(masking Not Used)
入排标准
- 年龄范围
- 18age old over 至 No limit(—)
- 性别
- All
入选标准
- •Patients aged 18 years and over who meet the diagnostic criteria for NTM pulmonary disease of the Japanese Society for Tuberculosis and Japanese Respiratory Society
- •Patients with SNAQ score of 14 or less or who are judged by the principal investigator (subinvestigator) to have insufficient food intake
- •Patients with BMI<20 and more than 2% weight loss within 24 months
- •Patients who have given their written consent to participate in this study
排除标准
- •Patients with other respiratory diseases with unstable symptoms (chronic obstructive pulmonary disease, asthma, etc.)
- •Patients with confirmed or suspected active malignancy
- •Patients with diabetes mellitus
- •Patients with a history of gastrectomy
- •Patients with unstable gastrointestinal disease
- •Patients with serious hepatic dysfunction (AST or ALT level of at least 3 times the institutional reference value within 3 months of obtaining consent)
- •Patients receiving continuous drug treatment for NTM pulmonary disease within 6 months(Discontinuation of amikacin injection or amikacin liposome inhalation suspension is not considered as a change in treatment)
- •Patients with a history of hypersensitivity to any component of the study drug
- •Patients with a history of taking Kampo medicines 2 weeks before the date of main registration
- •Patients who are taking oral or injection steroids
- •Patients who are pregnant or may become pregnant during the study period or who are breast-feeding
- •Patients who are participating in other clinical trials or have completed their participation within 1 month
- •Patients who are deemed ineligible by the investigator's judgment
结局指标
主要结局
-
Change in body weight before and after treatment (baseline to 24 weeks)
次要结局
- Body weight(baseline to 12 and 24 weeks)
- BMI(baseline to 12 and 24 weeks)
- SNAQ(baseline to 12 and 24 weeks)
- SF-36(baseline to 12 and 24 weeks)
- CAT(baseline to 12 and 24 weeks)
- mMRC(baseline to 12 and 24 weeks)
- Muscle mass (lean body mass)(baseline to 12 and 24 weeks)
- Fat mass(baseline to 12 and 24 weeks)
- Blood biochemical tests: active ghrelin, inactive gherelin, adiponectin, leptin, TNF-a, IL-6, albumin, prealbumin(baseline to 12 and 24 weeks)
研究者
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