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Clinical Trials/ChiCTR2200057581
ChiCTR2200057581Not yet recruitingNot Applicable

衰弱对射血分数保留的心力衰竭非常规就诊等不良预后的影响

自筹1 site in 1 countryStarted: October 31, 2021Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Locations
1
Primary Endpoint
非常规就诊

Study Overview

Brief Summary

探讨衰弱对于射血分数保留的心力衰竭患者非常规就诊等不良预后的影响

Study Design

Study Type
干预性研究
Primary Purpose
队列研究

Eligibility Criteria

Ages
60 to — (—)
Sex
All

Inclusion Criteria

  • 超声评估 LVEF≥50%;
  • 配合进行老年综合评估及超声心动图检查;

Exclusion Criteria

  • 严重急性失代偿期心力衰竭、严重心脏瓣膜病、先天性心脏病、急性心肌梗死;
  • 严重感染性疾病、甲亢、自身免疫性疾病;
  • 合并严重膝关节或髋关节骨关节炎、腰椎管狭窄、帕金森病或帕金森综合征;
  • 慢性呼吸疾病或 CTEPH 等其他可导致肺动脉高压的疾病。

Outcomes

Primary Outcomes

非常规就诊

Time Frame: 12 个月

全因死亡

Time Frame: 12 个月

Secondary Outcomes

  • 主要心血管事件(12 个月)

Investigators

Sponsor
自筹

Study Sites (1)

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