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临床试验/NCT05736237
NCT05736237已完成不适用

Identification and Verification of Candidate Genes Responsible for Optic Disc Drusen

Copenhagen University Hospital at Herlev1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2023年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20
试验地点
1
主要终点
Candidate gene

研究概览

简要总结

The goal of this observational study is to learn about the genetic background for the development of optic disc drusen. The main question is:

• Can one or more candidate genes be found?

Participants will have a blood sample taken and answer a questionnaire.

详细描述

The study is an international collaboration between University of Utah, University of Sydney, University of Valladolid, and University of Copenhagen. Patients with Optic disc drusen from 15 known optic disc drusen-families from different countries (USA, Australia, Spain and Denmark) are participating in this study.

Blood samples are drawn from each patient and their affected and unaffected family members, and DNA will be extracted. The investigators will do an Optical coherence tomography-scan (according to ODDS Consortium guidelines), and the participant will be asked to fill out the Visual Function Questionnaire (VFQ-25) including four additional questions about optic disc drusen.

The etiology of optic disc drusen will be analyzed with a Whole Exome Sequencing (WES), with the use of Next Generation Sequencing (NGS). Prior to WES, all participants will receive genetic counseling by a consultant to ensure awareness of possible secondary genetic findings.

研究设计

研究类型
Observational
观察模型
Family Based
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients over the age of 18, who are capable of giving consent
  • Diagnosis of optic disc drusen and a minimum of 3 optic disc drusen-affected family members

排除标准

  • Less than 3 affected family members
  • Under the age of 18 or mentally disabled

结局指标

主要结局

Candidate gene

时间窗: 2023-2024

Genetics variants shared by the families will be compared with findings in the remaining families and identical genes will undergo further analysis.

次要结局

未报告次要终点

研究者

发起方
Copenhagen University Hospital at Herlev
申办方类型
Other
责任方
Principal Investigator
主要研究者

Alvilda Steensberg

Principal Investigator

Rigshospitalet, Denmark

研究点 (1)

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