跳至主要内容
临床试验/DRKS00016158
DRKS00016158招募中不适用

Genetic screening of an at-risk population for Hereditary TransthyRetin-related AMyloidosis and longitudinal monitoring of TTR positive subjects - TRAMmoniTTR

Centogene AG Rostock0 个研究点目标入组 5,000 人开始时间: 2019年3月12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
5,000

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

  • Informed consent is obtained from the participant
  • The participant has no diagnosis of alcoholism according to international guidelines
  • The participant has not undergone chemotherapy for any carcinoma
  • The participant is at risk for hATTR due to two or more the factors listed below:
  • - cardiomyopathy or polyneuropathy with no obvious etiology
  • - atypical Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) or Motor Neuron Disease (MND)
  • - autonomic dysfunction
  • - hypertrophic cardiomyopathy or heart failure with preserved ejection fraction Left Ventricular Hypertrophy (LVH)
  • - bilateral carpal tunnel syndrome
  • - spinal stenosis or spinal radiculopathy
  • - gait disorders
  • - ocular changes involving vitreous opacities
  • - unexplained weight loss >5kg
  • - renal abnormalities
  • - family history of hATTR
  • - based on imaging or biopsy suspected for the wild type TTR (ATTR) and not genetically tested for hATTR
  • The participant is diagnosed with hATTR
  • The participant is a 1st or 2nd degree relative of the TTR positive subject

排除标准

  • Informed consent is not obtained from the participant
  • The participant is younger than 18 years of age
  • The participant has a diagnosis of alcoholism according to International guidelines
  • The participant has undergone chemotherapy for any carcinoma
  • The participant is not at risk for hATTR

研究者

发起方
Centogene AG Rostock

相似试验