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临床试验/CTRI/2019/08/020763
CTRI/2019/08/020763已完成2 期

Clinical evaluation of Jirakadyarishta in the management of Grahani

Central Council for Research in Ayurvedic Sciences CCRAS New Delhi0 个研究点目标入组 51 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
51

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 18-65 years
  • 2.Known cases of Grahani (diagnostic criteria as per classical Ayurvedic parameters)
  • a) Chronic or recurrent abdominal discomfort or pain
  • b) Abdominal bloating
  • c) Constipation
  • d) Diarrhoea
  • e) Urgency of bowel movements
  • f) Feeling of incomplete evacuation
  • g) Passage of mucus
  • 3.Patients willing to give written informed consent and able to participate for 3 months.

排除标准

  • 1.Patients with history of Inflammatory Bowel Disease (IBD), Kochââ?¬•s abdomen, Gluten intolerance.
  • 2.Patients with history of chronic Amoebiasis.
  • 3.Known cases of Diabetes Mellitus.
  • 4.Patients with poorly controlled Hypertension ( >160/100 mmHg)
  • 5.Patients who have history of Atrial Fibrillation, Acute Coronary Syndrome, Myocardial Infarction, Stroke or Severe Arrhythmia in the last 6 months
  • 6.Symptomatic patients with clinical evidence of Heart failure
  • 7.Known cases of malignancy
  • 8.Patients with concurrent serious hepatic disorders (defined as Aspartate Amino Transferase (AST) and / or Alanine Amino Transferase (ALT) > 2 times upper normal limit) or Renal Disorders (defined as S. Creatinine >1.2mg/dL), Severe Pulmonary Dysfunction (uncontrolled Bronchial Asthma and / or Chronic Obstructive Pulmonary Disease (COPD).
  • 9.Women who are planning for conception / pregnant or lactating.
  • 10.H/o hypersensitivity to any of the trial drugs or their ingredients
  • 11.Patients who have completed participation in any other clinical trial during the past three months
  • 12.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 New Delhi

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