EUCTR2009-018074-56-GB进行中(未招募)不适用
Revival of autochthonous adrenocortical stem cells in autoimmune Addison’s disease (RoSA) - Revival of Stem cells in Addison's disease (RoSA)
ewcastle upon Tyne Hospitals NHS Foundation Trust0 个研究点目标入组 12 人开始时间: 2010年3月18日最近更新:
适应症
相关药物
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
- •- Subjects between 16 and 65 years of age
- •- Adrenocortical failure, as judged by a basal cortisol of less than 100nmol/l or peak ACTH-stimulated cortisol response of less than 300nmol/l that was established a minimum of 1 year previously and persists at run-in assessments
- •- Elevation of ACTH at diagnosis or during testing in the run-in phase of the study
- •- Positive adrenal antibodies at baseline or recorded during illness
- •- Normal or atrophic adrenal glands on CT scan
- •- Willingness to travel to Newcastle CRF for study
- •- Willingness to attend education sessions about indications for parenteral glucocorticoid administration and technique of administration
- •- Female participants of child-bearing age will be willing to take acceptable contraception during study, and for 3 months following last synacthen dose
- •Are the trial subjects under 18? yes
- •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) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- Significant cardio-respiratory, chronic renal or non-autoimmune liver disease; malignancy
- •- Pregnancy, breast feeding or plan for pregnancy within 9 months
- •- Known non-autoimmune cause for adrenal failure (haemorrhage, adrenoleukodystrophy etc.)
- •- Known hypersensitivity or allergy to Synacthen, synacthen depot or zinc salts
研究者
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