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临床试验/NCT01619553
NCT01619553招募中不适用

Identification of Genetic Variants That Contribute to Keloid Formation in Families and Isolated Cases.

UConn Health2 个研究点 分布在 1 个国家目标入组 7,000 人开始时间: 2009年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
7,000
试验地点
2
主要终点
Identification of genetic elements

研究概览

简要总结

Keloids have a strong genetic component. The goal of this study is to identify genes and regulatory elements on chromosomes that are the cause for keloids or contribute to keloid scarring.

详细描述

Keloids are scars that keep growing beyond the border of the original wound. They typically persist for several years, expand for an extensive period of time and are sometimes called benign tumors. Keloids often have a lumpy surface and are often tender, itchy or inflamed around the growing border.

Keloids in most keloid patients do not run in the family. In the inheritable form of keloids it is possible that there is one major gene mutation that puts family members at risk for developing keloids. There may be other variations in the DNA (DNA makes up the chromosomes) that determine whether keloids become large and aggressive or stay small and without many symptoms.

For this study we will:

  • Send out study participation kits and consent by phone
  • Collect a saliva sample from eligible individuals
  • Obtain information regarding the keloids
  • Document keloids with photos
  • If keloid patients undergo keloid surgery we ask to obtain some scar tissue that would otherwise be discarded
  • Isolate DNA from the saliva sample
  • Perform genetic analyses of the DNA with the most up-to-date methods available to identify genetic variations
  • Study in the laboratory why the genetic variations cause keloids

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • unaffected individuals only if part of a participating keloid family

排除标准

  • no keloids;
  • unaffected individuals only as part of a participating keloid family

研究组 & 干预措施

affected

individuals with keloids

unaffected

unrelated unaffected controls or unaffected family members

结局指标

主要结局

Identification of genetic elements

时间窗: at time of identification

The goal is to identify relevant genes or genetic elements that cause the disease or contribute to the disease progression and severity.

次要结局

未报告次要终点

研究者

发起方
UConn Health
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ernst Reichenberger

Associate Professor

UConn Health

研究点 (2)

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