EUCTR2011-003541-17-ES进行中(未招募)1 期
EFFECT OF THE ADMINISTRATION OF ALLOPURINOL ON THE PREVENTION OF MUSCLE MASS LOSS IN IMMOBILIZED SUBJECTS.
Instituo de Investigacion Sanitaria La Fe0 个研究点开始时间: 2011年10月28日最近更新:
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
- •Patients with grade II sprain.
- •Ages 20 to 40 years.
- •Patients not taking regular medication. The concept is understood not to take regular medication to all patients who chronically fail to take any medication in a timely manner regardless of whether they needed to take the last week or last month for a condition treatment on time.
- •All patients must have written full informed consent specifically for this study
- •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 50
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Liver and gastrointestinal disease.
- •Hipotiroismo untreated.
- •Alcohol and / or substance abuse.
- •Vitamin supplements.
- •Eating disorders.
- •Drugs that lower lipid levels.
- •Hypotensive drugs.
- •Athletes who perform strenuous exercise.
- •Mental disorders, depression or anxiety intensity. These diseases cause the patient unable to understand the nature or scope and possible consequences of the study.
- •Patients with any infectious process and / or inflammatory before collecting the sample.
- •Patients may not follow the protocol because of its lack of cooperation, inability to return to subsequent visits and there is little chance of completing the study procedures.
- •Hypersensitivity to allopurinol.
研究者
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