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临床试验/NCT02240043
NCT02240043已完成不适用

Growth Hormone Evaluation in the Elderly People

Universidade Federal do Rio de Janeiro0 个研究点目标入组 48 人开始时间: 2011年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
48
主要终点
Growth Hormone Secretion in the elderly people using glucagon stimulation test (GST)

研究概览

简要总结

The aim of this study is to evaluate the growth hormone (GH) and adrenocorticotrophic hormone (ACTH) secretion in elderly without hypothalamic-pituitary disease using the glucagon stimulation test (using Glucagen® Hypokit, Novo Nordisk A/S, Denmark) and evaluate some parameters such as sarcopenia, nutritional state, bone mineral density, frailty criteria with secretion of GH.

详细描述

subjects over 65 years old were recruited from the geriatric ambulatory unit of our hospital to voluntarily participate in a research study concerning the GH and ACTH axis in the elderly, which included the realization of the glucagon stimulation test as the first phase of the study.

The GST (Glucagen® Hypokit, Novo Nordisk A/S, Denmark) was the chosen test to assess both ACTH and GH release because of its few known contraindications and mild side effects. It is a provocative test to evaluate GH and ACTH axis, i.e, a diagnostic test, without therapeutic effects.

研究设计

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

入排标准

年龄范围
65 Years 至 95 Years(Older Adult)
性别
All
接受健康志愿者

入选标准

  • elderly people above 65 years old with comorbidities peculiar to their age (such as hypertension, diabetes, dyslipidemia, parkinson disease) or without comorbidities

排除标准

  • pituitary disease, severe acute disease, terminal renal chronic disease, active malignant cancer, the presence of any other disease that could interfere with the somatotrophic axis evaluation, and the contraindications for glucagon administration (pheochromocytoma, insulinoma and malnourishment).

结局指标

主要结局

Growth Hormone Secretion in the elderly people using glucagon stimulation test (GST)

时间窗: up to one week

次要结局

  • ACTH release in the elderly people using GST(up to one week)

研究者

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

Ana Beatriz Winter Tavares

MD

Universidade Federal do Rio de Janeiro

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