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临床试验/NCT02735824
NCT02735824招募中不适用

Genetic Study of Immunodeficiency: Search for New Genetic Causes for Primary Immunodeficiencies

University Children's Hospital, Zurich3 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2016年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
500
试验地点
3
主要终点
Number of patients with suspected PID for whom a genetic cause has been identified

研究概览

简要总结

Individuals with suspected primary immunodeficiency will be studied and the results compared with healthy controls. Primary immunodeficiency may manifest as recurrent, severe or unusual infections as well as signs and symptoms of immune dysregulation such as autoimmunity or lymphoproliferation.

详细描述

Patients with a suspected immunodeficiency will be identified and invited to participate. Upon agreement, an additional blood sample will be collected when they have their routine bloods taken. If the study participants undergoes anaesthesia for any other reason, a small skin biopsy will be taken as well. Additional samples including blood samples or mouth swabs will be taken from healthy family members. Blood from healthy controls will only be taken when there is a clinical need for blood sampling (or when the study participant is already anaesthetised for any other reason) and not for research purposes only.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients: Pediatric patients (in/outpatient or referred) with suspected or confirmed Inborn Errors of Immunity.
  • Relatives: Healthy or affected biological relatives of enrolled patients.
  • Controls: Healthy volunteers with no history of chronic immunological, inflammatory, or infectious disease.
  • Consent: Ability to provide signed informed consent (or guardian consent).

排除标准

  • 未提供

研究组 & 干预措施

Patients with suspected PID

From included patients with suspected primary immunodeficiency (PID), i.e. patients with recurrent/unusual infection, immune dysregulation and/or susceptibility to malignancies from whom consent to participate was obtained, nucleated blood cells and/or fibroblasts from skin biopsy will be used for genetic testing and functional assays. Blood serum will be used for antibody and cytokine measurement.

干预措施: Blood Sampling (Procedure)

Patients with suspected PID

From included patients with suspected primary immunodeficiency (PID), i.e. patients with recurrent/unusual infection, immune dysregulation and/or susceptibility to malignancies from whom consent to participate was obtained, nucleated blood cells and/or fibroblasts from skin biopsy will be used for genetic testing and functional assays. Blood serum will be used for antibody and cytokine measurement.

干预措施: Skin Biopsy (Procedure)

Patients with suspected PID

From included patients with suspected primary immunodeficiency (PID), i.e. patients with recurrent/unusual infection, immune dysregulation and/or susceptibility to malignancies from whom consent to participate was obtained, nucleated blood cells and/or fibroblasts from skin biopsy will be used for genetic testing and functional assays. Blood serum will be used for antibody and cytokine measurement.

干预措施: Mouth Swab or Saliva Collection (Procedure)

Healthy Relatives of Patients with PID

From healthy relatives of patients with suspected PID from whom consent to participate was obtained, nucleated cells will be used for genetic testing in order to compare their genetic information with the one form their relatives with suspected PID.

干预措施: Mouth Swab or Saliva Collection (Procedure)

Healthy Relatives of Patients with PID

From healthy relatives of patients with suspected PID from whom consent to participate was obtained, nucleated cells will be used for genetic testing in order to compare their genetic information with the one form their relatives with suspected PID.

干预措施: Blood Sampling (Procedure)

Healthy Volunteers

From healthy volunteers from whom consent to participate was obtained, nucleated blood cells will be used for genetic testing and functional assays. Blood serum will be used for antibody and cytokine measurement. The data obtained will be compared to age matched patients with suspected PID.

干预措施: Blood Sampling (Procedure)

Healthy Volunteers

From healthy volunteers from whom consent to participate was obtained, nucleated blood cells will be used for genetic testing and functional assays. Blood serum will be used for antibody and cytokine measurement. The data obtained will be compared to age matched patients with suspected PID.

干预措施: Mouth Swab or Saliva Collection (Procedure)

结局指标

主要结局

Number of patients with suspected PID for whom a genetic cause has been identified

时间窗: Through study completion, an average of 3 years

Number of patients with suspected primary immunodeficiency included in the study for whom a diagnosis can be made with the genetic and functional data obtained from patients, their relatives and healthy volunteers.

次要结局

未报告次要终点

研究者

发起方
University Children's Hospital, Zurich
申办方类型
Other
责任方
Sponsor

研究点 (3)

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