NCT00443144已完成不适用
D3-Growth Hormone Receptor Polymorphism and Total Effect of Recombinant Human Growth Hormone on Growth in Girls With Turner Syndrome
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 试验地点
- 1
研究概览
简要总结
The protein polymorphism of the growth hormone receptor characterized by the genomic deletion of exon 3 has been linked to the magnitude of the first-year-growth response to growth hormone (GH) in girls with Turner syndrome.
Objective: to study the long-term effect of GH therapy in Turner syndrome in correlation to this GHR polymorphism in a mainly retrospective design (chart-review).
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 38 Months 至 14 Years(Child)
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Turner syndrome defined by a structural aberration or lack of the X chromosome.
- •Growth velocity less than 2 cm/year at the time of final analysis (= final height).
排除标准
- •Age <3.5 or >14 years at start of GH therapy,
- •GH peak serum levels < 8 ng/ml in two independent tests,
- •Thelarche at start or during the first year of treatment,
- •Oxandrolone therapy for any time and a duration of GH therapy less than 2 years.
研究者
Gerhard Binder
Pediatric Endocrinology
University Hospital Tuebingen
研究点 (1)
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