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Clinical Trials/ChiCTR2100050504
ChiCTR2100050504RecruitingUnknown

超声测量脑卒中患者膈肌厚度及膈肌移动度的信度效度研究

Not provided1 site in 1 countryStarted: August 26, 2021Last updated:
Conditions

Trial Snapshot

Phase
Unknown
Status
Recruiting
Locations
1
Primary Endpoint
膈肌移动度

Study Overview

Brief Summary

主要目的: 1.完善超声测量脑卒中患者不同呼吸时相膈肌厚度及膈肌移动度的信度和效度研究; 2.探讨影响脑卒中患者膈肌厚度、膈肌测量的可能相关影响因素。

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18 to 80 (—)
Sex
All

Inclusion Criteria

  • •1.经 CT/MRI 确诊的脑卒中;
  • •3.年龄 18-80 岁;
  • •5.意识清楚,无明显认知障碍(简易智力检测量表(abbreviated mental test score, AMTS)≥8 分),能够听从指令并配合评估;
  • •6.患者或家属签署知情同意书。

Exclusion Criteria

  • •1.合并支气管哮喘、慢性阻塞性肺疾病等呼吸系统疾病;
  • •2.伴有胸膜疾病或胸廓畸形、胸腔 / 腹腔占位病变、神经肌肉接头疾病、急性或慢性疼痛影响呼吸动度等情况;
  • •3.胸部或腹部手术史;
  • •4.合并其他严重的躯体性疾病;

Outcomes

Primary Outcomes

膈肌移动度

膈肌厚度

信度,可重复性,效度

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Not provided

Study Sites (1)

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