EUCTR2004-002991-40-Outside-EU/EEA进行中(未招募)不适用
Evolution of Growth Rate in Children Suffering From aDisease Associated With Growth Retardation and Treated byGenotonorm. A Pilot Study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
- Pfizer Inc
- 入组人数
- 46
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1. For GH treatment issue bone age should be less than (<) 13 years for a boy and < 11 years for a girl.2. Naïve child: with measured height should be < 2.5 SD for chronological age (CA).
- •Child currently treated by GH should have annual growth rate greater than equal to (>=) +1 SD and measured height <-2.5 SD for CA at the time GH was started.
- •3. Documented disease or pathological conditions known to be associated with growth
- •retardation and/or an adult height < -2 SD.
- •4. Children with the same pathological condition or disease.
- •5. Genotonorm treatment can be initiated by a physician according to the French SCP. that is to say a physician working in a hospital pediatric department or in a hospital endocrinology and metabolic disease department and, who is a pediatrician and/or a pediatric endocrinologist
- •6. The child benefits of the French social security cover.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 46
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1. Idiopathic short stature.
- •2. Pathological condition or disease for which GH treatment is already approved in France.
- •3. Glucose intolerance on an oral glucose tolerance test dated less than 3 months or diabetes mellitus.
- •4. Syndrome known to be associated with an increased risk of cancer example. family history of adenomatous polyposis.
- •5. Participation in any other studies involving investigational or marketed products, concomitantly or within 30 days prior to entry in the study.
- •6. Unable and/or unlikely to comprehend and/or follow GH treatment and/or the
- •7. A previous history of intolerance or hypersensitivity to the study drug, or to drugs with similar chemical structures.
- •8. Subjects who are known or are suspected allergic to the preservative metacresol.
- •9. Pharmacological treatment with steroids for 1 year or more.
研究者
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