临床试验/NCT00623116

NCT00623116Unknown不适用

Kallmann Syndrome in Finland

Hospital for Children and Adolescents, Finland1 个研究点分布在 1 个国家目标入组 50 人开始时间: 2007年12月1日最近更新: 2008年2月25日

适应症

试验速览

阶段: 不适用
发起方
入组人数: 50
试验地点: 1
主要终点: Clinical features including quality of life, reversibility and genetic features of Kallmann syndrome in Finland

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

Objective is to characterize epidemiology, clinical and genetic features of Kallmann syndrome in Finland.

详细描述

Kallmann syndrome is comprised of idiopathic hypogonadotropic hypogonadism and anosmia (inability to smell). Associated phenotypes may include cryptorchidism, microphallus, bone deformations, mirror movements, hearing loss and infertility. Objective is to characterize epidemiology, clinical and genetic features of Kallmann syndrome in Finland.

研究设计

研究类型: Interventional
分配方式: Na
干预模型: Single Group
主要目的: Treatment
盲法: None

入排标准

年龄范围: 15 Years 至 —（Child, Adult, Older Adult）
性别: All
接受健康志愿者: 是

入选标准

•Kallmann syndrome
•Age 15 yrs or more

排除标准

•Severe mental retardation

结局指标

主要结局

Clinical features including quality of life, reversibility and genetic features of Kallmann syndrome in Finland

时间窗: 0, 3 mo and during subsequent F/U

次要结局

epidemiology(by 2012 (anticipated))

研究者

发起方

Hospital for Children and Adolescents, Finland

申办方类型

Other

研究点 (1)

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