Evaluation of efficacy and safety of Micellar Iron in the treatment of Iron Deficiency Anaemia patients: A prospective, randomised, double-blind, single centre, placebo-controlled, interventional study

Amitojas Wellness Private Limited0 个研究点目标入组 0 人开始时间: 待定最近更新: 2021年11月24日

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•1. Male and female subjects aged 18 years and above.
•2. Male subjects with haemoglobin level below 13.0 g/dL and female subjects with haemoglobin level below 12.0 g/dL.
•3. Subjects willing to provide informed written consent.

•1. Pregnant, planning to become pregnant or breastfeeding women.
•2. Subjects with anaemia other than iron deficiency anaemia.
•3. Subjects have undergone blood transfusion or underwent iron therapy in the last three months.
•4. Subjects with microcytic iron-overloading disorder (thalassemia, sideroblastic anemia)
•5. Current or past history of a serious illness including, seizures, major psychiatric illness, structural brain disease, liver or kidney failure, organ transplantation, rheumatoid arthritis, uncontrolled hypertension, uncontrolled diabetes or malignancy, cardiovascular event in the last three months.
•6. Alcohol or substance abuse
•7. Allergy or sensitivity to any of the ingredients in the study treatment
•8. Subjects who have participated in other clinical studies during the past 3 months or subjects who intend to participate in other clinical studies parallelly
•9. Subjects with any other illness or health condition which in the opinion/medical judgement of the study investigator makes the subject ineligible to participate in the study.

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