DRKS00034600招募中不适用
Immunological characterization of peripheral blood samples inpatients with pulmonary cachexia
MU Klinikum, Medizinische Klinik und Poliklinik V0 个研究点目标入组 80 人开始时间: 2024年7月9日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 80
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 one(—)
- 性别
- All
入选标准
- •underlying disease currently assumed to be stable, no emergency treatment with hospitalization >24 h in the last 4 weeks
- •- no antibiotic or hematopoietic (G-CSF) treatment in the last 4 weeks
- •- patient is able to read and answer questionnaires
- •- patient is able to perform lung function and diffusion measurement
- •- Patient able to perform a hand force measurement
排除标准
- •- patient age <18 years, patient not capable of giving informed consent
- •- unclear primary diagnosis (e.g.: suspected COPD, inclusion in the study can be reconsidered if the diagnosis is confirmed)
- •-severe known comorbidity associated with the development of cachexia, e.g. second malignancy, HIV infection (exception: concomitant COPD in NSCLC)
- •- Lack of weight gain during childhood development with a long-term low BMI <20 kg/m2
- •- known serious eating disorder, e.g. anorexia nervosa
- •- currently desired weight loss, e.g. as part of a diet
- •- anamnestic or documented Covid-19 infection within the last month
- •- pregnancy
- •- known critical anemia (Hb <8 g/dl)
- •- known high-grade cardiac arrhythmia
- •- known or documented allergy to nonivamide/nicobixil, as well as electrode patches
- •- after implantation of automatic, electronic devices, e.g. pacemakers
- •- after heart transplantation, lung transplantation
研究者
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