跳至主要内容
临床试验/CTRI/2024/07/070131
CTRI/2024/07/070131尚未招募3 期

A single arm clinical study to evaluate the efficacy of kalyanaka guda in the management of irritable bowel syndrome with special reference to vatika grahani - nil

ational Institute of Ayurveda, Deemed to be University, Jaipur0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方

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 between the age group of 18 to 60 years.
  • 2.Patients irrespective of sex and socio- economic status.
  • 3.Patients having signs and symptoms (abdominal pain and altered bowel habits) of
  • Irritable Bowel Syndrome and Vatika Grahani like parshvavankshanruk, chiraat dukham drav shushkam tanu..punah punah srujeta varchah..

排除标准

  • 1. Mixed infection with parasites like round worms, hook worms etc.
  • 2. Patients with bleeding per rectum.
  • 3. Patients with evidence of malignancy.
  • 4. Patients having concomitant illness like hypertension, diabetes mellitus type II,
  • Amoebic dysentery, Ulcerative colitis, Malabsorption syndrome,
  • Inflammatory Bowel Diseases & Intestinal tuberculosis, Lactase deficiency
  • 5. Patients suffering from major systemic illness like cancer, crohn’s disease, renal
  • failure etc.
  • 6. Patients who are taking corticosteroids, antidepressants, anticholinergic, or
  • any other drugs that may have an influence on the outcome of study.
  • 7. Alcoholics and drug abusers.
  • 8. Pregnant and lactating women.
  • 9. Patients who have completed participation in any other clinical trial during the
  • past six months.

研究者

发起方
ational Institute of Ayurveda, Deemed to be University, Jaipur

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