EUCTR2015-000578-37-NL进行中（未招募）1 期
The effect of Nandrolone Decanoate Injection and Leucine Supplementation on Muscle Loss During Immobilisation - Le-Na
Maastricht University Medical Centre+0 个研究点开始时间: 2015年4月13日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
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
- Male
入选标准
- •Aged from 18-35 years
- •18.5 < BMI < 30 kg/m2
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 30
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •(Family) history of thromboembolic events
- •Recent surgery (within 6 months prior to the study)
- •Performing progressive resistance training more than three times per week in the past year
- •Any back/leg/knee/shoulder complaints which may interfere with the use of crutches
- •Current systemic use of corticosteroids, anabolic steroids, growth hormone, testosterone, nandrolone, protein supplements, immunosuppressants or insulin, blood sugar decreasing medication or EPO
- •All co-morbidities interacting with mobility and muscle metabolism of the lower limbs (e.g. arthritis, spasticity/rigidity, all neurological disorders and paralysis)
- •Use of anti-coagulants
- •Pre-existing renal disease or those with a potential risk for renal dysfunction (diabetes, hypertension, reduced glomerular filtration rate)
- •Liver disease
- •Heart failure
- •Allergy to nuts or soy
- •High blood pressure (>140 mmHg systolic and >90 mmHg diastolic)
- •In case of doubt, in- or exclusion of subject will be discussed with responsible physician or principal investigator.
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