跳至主要内容
临床试验/DRKS00034600
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

发起方
MU Klinikum, Medizinische Klinik und Poliklinik V

相似试验