CTRI/2021/08/035488已完成3 期
CLINICAL EVALUATION OF SIDDHA HERBAL FORMULATION NELLI MULLI ILAGAM IN THE TREATMENT OF PITHA PAANDU (IRON DEFICIENCY ANAEMIA)
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Primary outcome will be assessed by comparing the pre and post treatment status of Peripheral smear and Haemoglobin level of the study subjects.
研究概览
简要总结
It is an interventional study in which 30 patients with any of the symptoms like pallor of skin, excessive thirst, giddiness, chest tightness, breathlessness, pungent or bitter taste, angular stomatitis, glossitis, fatigue will be selected based on inclusion and exclusion criteria. After enrolling the patients in the study, Nelli mulli ilgam 8 gram will be given twice a day for 48 days. After 48 days, patients will be asked to do blood investigations for any changes in it and absence of clinical signs and symptoms of Pitha paandu.
研究设计
- 研究类型
- Interventional
- 分配方式
- Not Applicable
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 14.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients with appropriate symptoms like pallor of skin, excessive of thirst, fatigue, blurred vision, giddiness, chest tightness, breathlessness, pungent or bitter taste, angular stomatitis, glossitis, cheilosis Hb level less than normal range, For male: 9-11gms/d1 For female: 8-10gms /dl Abnormal peripheral smear study – Microcytic Hypochromic Anaemia Patient willing to undergo blood investigation.
排除标准
- •Presence of any associated severe systemic illness like cancer, AIDS Chronic Kidney Disease Diabetes Mellitus Pregnant women Inherited defects like Sickle cell anaemia, Thalassemia, Aplastic anaemia Patients not willing to give blood sample.
结局指标
主要结局
Primary outcome will be assessed by comparing the pre and post treatment status of Peripheral smear and Haemoglobin level of the study subjects.
时间窗: 1 year
次要结局
- Reduction of clinical symptoms(Improvement in complete blood count)
研究者
研究点 (1)
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