CTRI/2023/05/052496尚未招募2 期
Efficacy and Safety of Punarnavadi Mandura and Dadimadi Ghrita Vs Standard Care in Adolescents with Iron Deficiency Anemia in Improving Hemoglobin Level, Functional Gut well-being and Cognitive Performance- A Randomized Active Controlled Trial
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
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
入选标准
- •1.Subjects of either sex aged between 12 and 18 years.
- •2.Subjects of either sex having Hemoglobin levels between 8-11gm%
- •3.Willing and able to participate in the trial
排除标准
- •Exclusion Criteria:
- •1. Subjects suffering from any other type of anemia such as Anemia of chronic diseases, megaloblastic anemia, sideroblastic anemia, hemolytic anemia
- •2. Any inherited blood disorder such as Thalassemia, aplastic anemia, sickle cell anemia
- •3. A history or a diagnosis of Acute myelogenous or lymphoblastic leukemia, Multiple myeloma, Primary or secondary myelodysplastic syndrome, hemochromatosis
- •4. Use of any iron-containing drugs or treatment for anemia during the last 3 months.
- •5. Known hypersensitivity to oral iron or any component of the trial intervention
- •6. Participants with conditions necessitating parenteral iron therapy such as impaired absorption due to diseases such as inflammatory bowel disease, blood loss, etc.
- •7. Subjects with evidence of malignancy, chronic infectious diseases, auto immune diseases
- •8. Patients on prolonged ( > 6 weeks) medication with corticosteroids, antidepressants, anticholinergics etc. or any other drugs that may have an influence on the outcome of the study.
- •9.Patients with concurrent serious hepatic disorder or Renal Disorders Severe Pulmonary Dysfunction or cardiac diseases.
- •10. Patients who have completed participation in any other clinical trial during the past six (06) months.
- •11. Any other condition which the Investigator thinks may jeopardize the study
研究者
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