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临床试验/NCT01797718
NCT01797718已完成2 期

Constitutional Delay of Growth and Puberty: Towards Evidence-based Treatment

Helsinki University Central Hospital4 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2013年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
35
试验地点
4
主要终点
testicular volume

研究概览

简要总结

Boys with constitutional delay of growth and puberty (CDGP) should be offered evidence-based effective and safe treatment option. This study compares the effects of low-dose testosterone and aromatase inhibitor letrozole on pubertal progression. The hypothesis is that, in boys CDGP showing earliest signs of puberty, peroral letrozole (2.5 mg/d for 6 mo) induces faster biochemical and clinical progression of puberty as compared to low-dose intramuscular testosterone Rx (~1mg/kg/mo for 6 mo). In addition, 10 or more boys who select watchful waiting instead of medication will provide background data on the natural progression of CDGP, and their data will not be used in primary statistical comparisons.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
14 Years 至 17 Years(Child)
性别
Male
接受健康志愿者

入选标准

  • Constitutional delay of growth and puberty
  • Age 14 years or more
  • mean testicular volume 2.5 ml or more and less than 4 ml
  • serum testosterone level less than 5 nM OR
  • as above, but serum testosterone 1 nM or more with normal DHEAS level, even if the mean testicular volume is less than 2.5 ml OR
  • as above, but tanner stage G2 and testosterone level less than 3 nM

排除标准

  • Chronic diseases
  • Primary or secondary hypogonadism
  • Chromosomal anomalies
  • Chronic medication that potentially adversely affects bone mineralization (excluding inhaled corticosteroid treatment)

研究组 & 干预措施

Testosterone

Active Comparator

~1mg/kg every 4 weeks for 6 months

干预措施: Testosterone (Drug)

Letrozole

Active Comparator

2.5mg daily for 6 months

干预措施: Letrozole (Drug)

结局指标

主要结局

testicular volume

时间窗: one year

Testes will be measured with a ruler to the nearest millimeter and volume will be calculated at 0, 6, and 12 mo

clinical and biochemical measures of pubertal progression

时间窗: one year

Activity of the hypothalamic-pituitary-gonadal axis, evaluated by * genital and pubic hair stage of puberty according to Tanner; * growth velocity (cm/yr); * basal and gonadotropin-releasing hormone (GnRH)-stimulated gonadotropin levels; * urinary luteinizing hormone levels; * testosterone; * inhibin B; * anti-mullerian hormone (AMH)

次要结局

  • Bone health(one year)
  • Psychosocial well-being(one year)
  • Puberty-related metabolical and clinical changes(one year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Tero Varimo, MD, PhD

MD

Helsinki University Central Hospital

研究点 (4)

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