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临床试验/PACTR202209576526787
PACTR202209576526787招募中4 期

A comparative study of the efficacy and safety of Hemoforce Family in the treatment of iron deficiency anaemia in a tertiary healthcare facility in Northern Ghana.

Shalina Healthcare0 个研究点目标入组 200 人开始时间: 2022年9月21日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
13 Year(s) 至 18 Year(s)(—)
性别
All

入选标准

  • Male or female (=12 years) suffering from iron deficiency anaemia having hemoglobin between 9 to 12 g/dl.
  • Patients or parents willing to provide written informed consent to use personal and/or health data prior to the entry into the study.

排除标准

  • Anaemia not linked to iron deficiency.
  • Hemoglobin less than 9 g/dL.
  • Allergy to iron derivatives.
  • Any medical disorder like diabetes or tuberculosis (TB), viral hepatitis cirrhosis, renal disease, autoimmune disease.
  • Those who had received parenteral iron treatment earlier within 3 months before the start of the study.
  • Patients with history of chronic blood loss.
  • Alcohol abuse within past 6 months.
  • Hemosiderosis, hemochromatosis or other iron storage disorders.
  • Patients with a history or present illness that is a malignant tumor or autoimmune disease.
  • Patients who underwent oral administration of an iron preparation (including an over-the-counter drug or supplement) within 4 weeks before the screening.

研究者

发起方
Shalina Healthcare

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