EUCTR2017-005110-58-NL进行中（未招募）1 期
Efficacy of a predefined vitamin D dosing regimen in vitamin D-insufficient multiple myeloma patients. - Efficacy of vitamin D supplementation in multiple myeloma patients.
Medical Centre Leeuwarden0 个研究点目标入组 40 人开始时间: 2018年5月14日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 40
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 are (newly) diagnosed with smoldering or symptomatic multiple myeloma. Subjects must be over 18 years of age. Subjects must be able to give informed consent. Subjects with a 25-hydroxyvitamin D level =75 nmol/l.
- •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 11
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 29
排除标准
- •Contraindications for the use of vitamin D: Hypersensitivity to the active substance(s) or to any of the excipients; Hypercalcaemia and/or hypercalciuria; Nephrolithiasis and/or nephrocalcinosis; Serious renal impairment; Hypervitaminosis D; Pseudohypoparathyroidism.
- •The use of vitamin D tablets or multivitamin tablets containing vitamin D
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