跳至主要内容
临床试验/CTRI/2014/10/005081
CTRI/2014/10/005081尚未招募2 期

A Clinical Evaluation of Triphala Guggulu and Kasisadi Taila in the management of Arsha (Haemorrhoids). - CETKMA

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
尚未招募
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 16 â??60 years.
  • 2.Presence of 1st, 2nd & 3rd degree Arsha (Hemorrhoids) confirmed by clinical / proctoscopic / colonoscopic examination (With or without bleeding / painful or painless).
  • 3.Willing and able to participate in the study for 06 weeks

排除标准

  • 1.Age below 15 years & above 60 years
  • 2.Thrombosed & Strangulated pile mass (Hemorrhoids)
  • 3.Bleeding diathesis
  • 4.Cirrhosis of Liver- Portal hypertension
  • 5.Ulcerative colitis / Crohnâ??s disease
  • 6.Patients with evidence of malignancy
  • 7.Patients on prolonged ( > 6 weeks) medication with corticosteoids, antidepressants, anticholinergics, immunosuppressants, estrogen replacement therapy etc. or any other drugs that may have an influence on the outcome of the study.
  • 8.Patients suffering from major systemic illness necessitating long term drug etc.
  • 9.Patients who have a past history of Atrial Fibrillation, Acute Coronary Syndrome,
  • 10.Myocardial Infarction, Stroke or Severe Arrhythmia in the last 6 months.
  • 11.Symptomatic patient with clinical evidence of Heart failure.
  • 12.Patients having uncontrolled Diabetes Mellitus (Blood Sugar Fasting > 250mg/dl).
  • 13.Patients with concurrent serious hepatic disorder (defined as aspartate aminotransferase (AST) and / or alanine aminotransferase (ALT), total bilirubin or alkaline phosphatase (ALP) > 2 times upper normal limit) or renal disorders (defined as S.creatinine >1.2mg/dL), severe pulmonary dysfunction (uncontrolled asthma and chronic obstructive pulmonary disease [COPD]), inflammatory bowel
  • 14.Disease or any other condition that may jeopardize the study..
  • 15.Pregnant/ lactating females.
  • 16. Patients on oral contraceptives.
  • 17.Alcoholics and/or drug abusers.
  • 18.H/o hypersensitivity to any of the trial drugs or their ingredients.
  • 19.Patients who have completed participation in any other clinical trial during the past six (06) months.
  • 20.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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