EUCTR2007-003114-34-BE进行中（未招募）不适用
The impact of oral curcumin (Curcuma longa) on mycophenolic acid and metabolite pharmacokinetics in stable renal allograft recipients: exploratory investigation of the role of intestinal uridine-diphosphate-glucuronosyltransferases (UGTs) in in vivo mycophenolic acid disposition.
Department of Nephrology and Renal Transplantation, University Hospitals Leuven0 个研究点目标入组 12 人开始时间: 2007年11月26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
- •Primary and secondary renal allograft recipients.
- •Stable (clinically and biochemically) renal transplant patients.
- •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
- •Age < 18 yrs of age.
- •Combined solid organ transplantations.
- •History of medical or surgical diseases of the gastrointestinal and hepato-biliary tract.
- •Recipients with active infectious or inflammatory disease as well as anti-infectious or anti-inflammatory treatment for at least 2 weeks prior to enrolment.
- •Severe hypoalbuminemia (< 25 g/L).
- •Severe anemia (< 8 g/dL).
- •Patients with documented non-compliance.
研究者
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