跳至主要内容
临床试验/NCT06527521
NCT06527521招募中不适用

Prevalence of Amyloidosis in Trauma Patients Using Red Flags Tool

Consorci Sanitari de l'Alt Penedès i Garraf1 个研究点 分布在 1 个国家目标入组 246 人开始时间: 2024年11月13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
246
试验地点
1
主要终点
Amyloidosis

研究概览

简要总结

This study aims to determine the frequency of amyloidosis among patients undergoing trauma surgery.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

性别
All
接受健康志愿者

入选标准

  • Men and women included in the waiting list for scheduled trauma surgery with at least one of the following criteria defined as red flags: Over 65 years old; Possible family history of amyloidosis, Cardiac pathology: aortic stenosis, presence of left ventricular hypertrophy defined as interventricular septal thickness > 12mm measured by echocardiography, history of previous brady- or tachyarrhythmias including cardiac conduction blocks, history of syncope or presyncope, pro BNP > 300 in previous blood tests; History of sensory peripheral neuropathy; History of nephropathy without etiological diagnosis; History of liver disease without a clear cause.
  • Ability to cooperate in the necessary evaluations.
  • Signed informed consent for inclusion in the study, either by the participant or their legal representative.

排除标准

  • - Participants previously diagnosed with amyloidosis cannot be included in the study.

结局指标

主要结局

Amyloidosis

时间窗: One month

Proportion of patients undergoing scheduled orthopedic surgery who are diagnosed with amyloidosis.

次要结局

未报告次要终点

研究者

发起方
Consorci Sanitari de l'Alt Penedès i Garraf
申办方类型
Other
责任方
Sponsor

研究点 (1)

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