跳至主要内容
临床试验/CTRI/2012/03/002524
CTRI/2012/03/002524招募中2 期

Clinical Evaluation of Punarnavadi Mandura and Dadimadi Ghrita in the Management of Iron Deficiency Anaemia - IMCRP â?? IDA â?? 2010 - 2011

Central Council for Research in Ayurvedic Sciences CCRAS0 个研究点目标入组 150 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
150

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) Patients of either sex aged between 15 to 60 years.
  • 2) Patients with iron deficiency anaemia (Hb 8gm-10gm.%),
  • 3) Patients with peripheral blood smear suggestive of Iron deficiency Anaemia
  • 4) Willing and able to participate for 14 weeks.

排除标准

  • 1. Patients suffering from Thalassemia major / Aplastic anaemia / Sickle cell anaemia.
  • 2. Patients with evidence of malignancy.
  • 3. Patients suffering from major systemic illness necessitating long term drug treatment
  • (Rheumatoid arthritis, Psycho-Neuro-Endocrinal disorders, Bleeding disorders, etc.)
  • 4. Patients who have a past history of Atrial Fibrillation, Coronary Artery Disease (CAD), Acute
  • Coronary Syndrome, Myocardial Infarction, Stroke or Severe Arrhythmia in the last 6 months.
  • 5. Symptomatic patient with clinical evidence of Heart failure.
  • 6. Patients with poorly controlled Hypertension ( > 160 / 100 mm Hg)
  • 7. Patients suffering from Diabetes Mellitus {B.S. (F) > 250 mg/dl.
  • 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 (defined as Aspartate Amino
  • Transferase (AST) and / or Alanine Amino Transferase (ALT), Total Bilirubin, Alkaline
  • Phosphatase (ALP) > 2 times upper normal limit), or Renal Disorders (defined as S. Creatinine
  • >1.2mg/dL), Total Serum Cholesterol & / or Serum Triglycerides > 250 mg/dl, Severe Pulmonary
  • Dysfunction (uncontrolled Bronchial Asthma and / or Chronic Obstructive Pulmonary Disease
  • 10. Alcoholics and/or drug abusers.
  • 11. Pregnant / lactating woman
  • 12 H/o hypersensitivity to the trial drug or any of its ingredients.
  • 13 Patients who have completed participation in any other clinical trial during the past six (06)
  • 14 Any other condition which the Investigator thinks may jeopardize the study.

研究者

发起方
Central Council for Research in Ayurvedic Sciences CCRAS

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