EUCTR2005-001768-30-SE进行中（未招募）不适用
Comparison of 2 and 4 doses hydrocortison substitution with regard to plasma concentration and quality of life. - CHEQ
EM-kliniken0 个研究点目标入组 12 人开始时间: 2005年12月7日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 12
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) Cortisol plasma level < 300 nmol/L during stimulation test
- •2) ACTH > 300 ng/L
- •3) Age > 18 years
- •4) Informed concent
- •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
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1) Chronic severe disease with risk of deterioration that can influence the cortisol substitution program
- •2) Chronic drug abuse
- •3) suspicion of non compliance
研究者
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