EUCTR2007-005244-25-DK进行中（未招募）不适用
Co-treatment with pegvisomant and a somatostatin analogue (SA) in SA-responsive acromegalic patients: impact on insulin sensitivity, glucose tolerance, and pharmacoeconomics
Aarhus University Hospital, Department M0 个研究点开始时间: 2007年10月31日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 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
- All
入选标准
- •Acromegalic patients on SA mono therapy, who are considered well-controlled.
- •1) a serum IGF-I < 2 SDS above the upper normal range or
- •2) a nadir GH < 0.5 µg/l.
- •3) Borderline patients, who do not entirely meet these criteria, may be included.
- •This could mean patients who have been on SA mono therapy with appropriate
- •symptom relief for more than 3 years.
- •Written consent
- •Age > 18 years
- •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
- •Known allergies to IMP
- •Known liver disease
- •Diabetes Mellitus type I
研究者
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