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临床试验/NCT02854397
NCT02854397终止不适用

Determination of Specific Biomarkers of Acute Attack of Angioedema Within Pediatric Population

University Hospital, Grenoble14 个研究点 分布在 1 个国家目标入组 31 人开始时间: 2016年2月15日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
31
试验地点
14
主要终点
VE-cadherin level

研究概览

简要总结

In emergency room, this is crucial to diagnose an acute attack of hereditary angioedema (HAE) to quickly provide the efficient treatment. Currently, there is no specific biomarker for acute attack of bradykinin-mediated angioedema to help clinicians for patient care. However, previous works are carried out for that purpose. All the potential candidate biomarkers must be validated in prospective studies to estimate their specificity and sensitivity values, and to understand their potential utility in patient care.

The main goal of this clinical trial is to estimate the diagnostic value of VE-cadherin in pediatric population, for the differential diagnosis between HAE crisis and angioedema resulting of mast cell activation crisis (the main differential diagnosis of HAE).

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
1 Year 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • For HAE: patient with a documented diagnosis of HAE:
  • type I (from an antigenic deficiency of the C1 esterase inhibitor) or type II (from a functional deficiency of the C1 esterase inhibitor). The existence of a mutation in SERPING1 was not necessary for the inclusion
  • HAE with normal C1-INH (ex type III) with a required mutation in FXII gene or with a typical family history of HAE diagnosed by a specialized physician belonging to CREAK network.
  • For AE resulting of mast cell activation: a documented diagnosis of AE resulting of mast cell activation included:
  • mastocytosis,
  • chronic spontaneous urticaria,
  • acute urticaria after exposure of allergen during allergy challenge tests,
  • mast cell activation syndrome.
  • For the control group:
  • composed of patients who presented a stabilized disease (that was not infectious, not auto-inflammatory or inflammatory disease and without implication of endothelial cells).

排除标准

  • Over 18 years or under 1 year.
  • Diagnosis of HAE with a normal C1 esterase inhibitor or AE of unknown aetiology.
  • Patients with HAE who received an acute attack treatment before the blood sample (the C1 esterase inhibitor concentrate or a bradykinin B2 receptor antagonist); patients with HAE who received a prophylactic treatment (danazol).
  • Patients who were treated by omalizumab or corticosteroid treatment.

结局指标

主要结局

VE-cadherin level

时间窗: Half a day

For the diagnosis of acute attack of hereditary angioedema

次要结局

  • Dosage of Fc KHPM(Half a day)
  • Dosage of VE-cadherin (vascular endothelial)(Half a day)
  • Dosage of D-dimer(Half a day)
  • Dosage of Tryptase(Half a day)

研究者

发起方
University Hospital, Grenoble
申办方类型
Other
责任方
Sponsor

研究点 (14)

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