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临床试验/NL-OMON40886
NL-OMON40886尚未招募4 期

Optimizing Iron suppletion trial after Roux- en -Y Gastric Bypass - Ironsuppletion trial

Rijnstate Ziekenhuis0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • All patients who underwent a gastric bypass and developped an irondeficiency postoperatively (ferritin< 20 microfram/l) ,age between 18-65 years

排除标准

  • iron deficiency preoperatve, bloodtransfusions during study period, ironcontaining nutritional supplements except the 'standard' multivitamins after bariatric surgery, decreased renal failure, excessive manstruational blood loss, anemia not caused by iron deficiency, accumulation of iron, hypersensitivity for one of the medicinal products, psychiatric illness, pregnancy.;Acute and chronic infection or other inflammationreactions, liver dysfunction.

研究者

发起方
Rijnstate Ziekenhuis

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