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临床试验/NCT01871714
NCT01871714已完成不适用

Phenotypic Properties in Individuals Affected With X-linked Hypohidrotic Ectodermal Dysplasia: Symptoms and Facial Recognition

Edimer Pharmaceuticals1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2013年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30
试验地点
1
主要终点
To collect demographic and clinical status information in XLHED-affected males, adult females at risk for XLHED and adult female controls

研究概览

简要总结

The current study design incorporates two previously developed, non-invasive approaches to characterize the phenotype of individuals affected with XLHED.

详细描述

The current study design incorporates two previously developed, non-invasive approaches to characterize the phenotype of individuals affected with XLHED. Facial 3-dimensional (3D) imaging will be created from white-field morphometric scanning (Hammond, 2004. The 3D facial photographs collected from males (ages 4 years and up) will be used to develop a non-invasive screening tool, which could enable detection of craniofacial signs of XLHED in the newborn period. 3D facial profiling has been reported to be effective in identifying HED (Dellavia et al., 2008), but the technology does not yet meet the ease-of-use criteria for a universal screening tool.

Standard 2-dimensional (2D) frontal and lateral facial photographs will be taken of the same XLHED-affected male subjects as well as of adult females (ages 18-45 yrs) at risk for being XLHED carriers and unaffected adult female controls. The 2D facial photographs will serve a dual purpose; the first being to beta-test a previously developed algorithm to identify males affected with XLHED (Automatic Phenotype Identification of XLHED Patients Final Report, December 25, 2012, unpublished), and the second to adapt the facial recognition algorithm to identify female carriers of XLHED.

研究设计

研究类型
Observational

入排标准

年龄范围
4 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Females of original gender of age 18-45 years who are registered and attending the 2013 NFED Family Conference. This will include those at risk for XLHED and controls
  • XLHED-affected males of original gender of age 4 yrs and up who are registered and attending the 2013 NFED Family Conference
  • Provide informed consent/assent

排除标准

  • Subjects who are not able or are not willing to comply with the procedures of this protocol
  • Subjects with any major medical problem that will prevent them from participating in this study
  • Male subjects who participated in the prior study ECP-003 sponsored by Edimer Pharmaceuticals Inc. in May 2011 in San Francisco, CA
  • Males at risk for XLHED with prior genetic testing that did not reveal an EDA mutation

结局指标

主要结局

To collect demographic and clinical status information in XLHED-affected males, adult females at risk for XLHED and adult female controls

时间窗: Study day 1

To collect demographic and clinical status information in XLHED-affected males, adult females at risk for XLHED and adult female controls using a medical questionnaire

To test and refine a computer algorithm for facial recognition of XLHED

时间窗: Study day 1

To test and refine a computer algorithm for facial recognition of XLHED based on 2D facial photographs obtained from subjects at risk for XLHED and controls

To evaluate 3-dimensional facial imaging technology for mapping craniofacial development in XLHED males

时间窗: Study day 1

To evaluate 3-dimensional facial imaging technology for mapping craniofacial development in XLHED males

To test for the presence of genetic mutations in subjects at risk for XLHED

时间窗: Study day 1

To test for the presence of genetic mutations in subjects at risk for XLHED who lack prior genetic diagnosis

To test the validity of a using saliva samples for genetic testing

时间窗: Study day 1

To test the validity of a using saliva samples for genetic testing buy simultaneously perform genetic testing on blood and salvia and comparing the mutations identified

次要结局

未报告次要终点

研究者

发起方
Edimer Pharmaceuticals
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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