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临床试验/KCT0009088
KCT0009088已完成未知

Clinical study comparing diagnostic rates between 24-hour Holter monitoringand portable ECG devices in Cardiogenic vertigo

Pusan National University Hospital0 个研究点目标入组 49 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
49

研究概览

简要总结

During the 72-hour monitoring period, there was no significant difference in the overall detection rate of arrhythmia events between the wearable patch and conventional Holter monitoring (21.3% vs.17.0%, P > .001). Most patients (46/47) favored a wearable patch over Holter monitoring. The detection of CV was associated with a lower frequency of vertigo. The effectiveness of wearable ECG patch monitoring was comparable to conventional Holter monitoring in detecting CV. With its extended monitoring capability and patient preference, wearable patch monitoring holds promise as an alternative method for CV diagnosis.

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19(Year) 至 o Limit(—)
性别
All

入选标准

  • 1. Patients with heart disease over 19 years of age
  • 2. Recurrent dizziness lasting less than 5 minutes
  • 3. Cases not explained by other neurological or neurotological diagnoses

排除标准

  • 1. Patients whose dizziness is determined to be caused by another vestibular disease such as vestibular neuritis or Meniere's disease
  • 2. Patients whose dizziness was found to be caused by an organic central disease.
  • 3. Patients who, in the judgment of the researcher, have clinically serious diseases (liver disease, kidney disease, malignant tumor, etc.) that make it difficult to participate in the study.
  • 4. Other patients who find it difficult to participate according to the researcher's judgment.
  • 5. Those who do not agree to participate in the study.

研究者

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