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临床试验/NCT04484051
NCT04484051尚未招募不适用

Growth Hormone Study in Adults With Prader-Willi Syndroom

Erasmus Medical Center1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2023年3月24日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
25
试验地点
1
主要终点
Change in lean body mass

研究概览

简要总结

The overall objective of this study is to measure the effect of growth hormone (GH) treatment on physical and psychosocial health in adults with Prader-Willi syndrome. Adults with PWS who have not been treated with GH during the past three years and who will start with GH treatment as part of regular patient care will be asked for informed consent to participate in this open-label prospective cohort study. We hypothesize that growth hormone treatment will improve the physical and psychosocial health.

详细描述

OBJECTIVES:

To measure the effect of GHt on physical and psychosocial health in adults with PWS.

The primary endpoint is change in lean body mass (LBM (kg)) as assessed by Dual Energy X-ray Absorptiometry (DEXA) scan. Secondary endpoints are total fat mass, bone density, physical health and psychosocial health. Also the occurrence of side-effects will be assessed. Only data that are collected as part of regular patient care will be used.

STUDY DESIGN:

Open-label prospective cohort study.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • The patient is diagnosed with Prader-Willi syndrome (genetically confirmed)

排除标准

  • Non cooperative behaviour
  • Pregnancy
  • Known malignancies
  • Poorly controlled diabetes (HbA1c > 64 mmol/mol (8%))
  • Untreated obstructive sleep apnea (apnea-hypopnea index > 5)
  • Body mass index above 40 kg/m2
  • Upper-airway obstruction of any cause

结局指标

主要结局

Change in lean body mass

时间窗: 36 months

Change in lean body mass (in kg) as measured by Dual Energy X-ray Absorptiometry scan

次要结局

  • Change in fat mass(36 months)
  • Change in bone density(36 months)
  • Change in physical strength(36 months)
  • Change in laboratory measurements(36 months)
  • Change in psychosocial functioning(36 months)
  • Change in caregiver burden(36 months)

研究者

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

dr. Laura C. G. de Graaff-Herder

MD, PhD

Erasmus Medical Center

研究点 (1)

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