EUCTR2007-004139-49-IT进行中（未招募）1 期
Efficacy and tolerability of 12-weeks oral treatment with V0355CP3A versus Ferrograd, in iron deficiency anaemia. Multicenter, randomised, open-label trial. - ND
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 300
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
入选标准
- •Ambulatory female between 18 and 50 years. Haemoglobin level between 90 g/L and 120 g/L. Serum ferritin level < 30 µg/L). Willing to participate. Able to understand the protocol, to comply with its requirements and to attend to visits. Have given their written informed consent to participate in the study;
- •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) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •For women with childbearing potential:
- •o not using effective contraception (oral contraceptives, intrauterine device, tubal
- •ligation or other efficient procedures ),
- •o pregnant, breast feeding or likely to become pregnant during the time of the study
- •o positive urinary pregnancy test.
- •Anaemia related to other causes than iron deficiency.
- •Inflammatory bowel disease or any digestive disease.
研究者
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