EUCTR2014-001444-37-NL进行中（未招募）不适用
Optimizing iron suppletion after Roux-en-Y Gastric Bypass
Rijnstate Hospital0 个研究点开始时间: 2014年4月23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
- •All patients who underwent a gastric bypass and develop a irondeficiency postoperatively. (ferritin< 20microgram/l) Age between 18 and 65 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 120
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •iron deficiency preoperative, bloodtransfusios during studyperiod, ironcontaining nutritional supplements except the 'standard' multivitamins after bariatric surgery, decreased renal failure, excessive menstruational blood loss, anemia not caused by irondeficiency, accumulation of iron, hypersensitivity for one of the medicinal products, psychiatric illness, pregnancy
研究者
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