跳至主要内容
临床试验/CTRI/2024/07/070382
CTRI/2024/07/070382尚未招募2/3 期

A randomized comparative clinical study to evaluate the efficacy of simhasyadi kwatha and patoladipanchanga kwatha in management of amlapitta

Dr Vijayalakshmi Teggi1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年7月16日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Effect of treatment will be assessed on the basis of changes found in the gradation of the both individual and overall parameters according to their severity before, during and after treatment.

研究概览

简要总结

This is a randomized comparative clinical study to evaluate the effect of two groups of kwatha in management of symptoms of amlapitta for 30 days this study comprise of two groups of 30 patients selected as per inclusion and exclusion citeria study will be Conducted in ALN Rao memorial ayurvedic hospitals in koppa and guard hullow places, koppa taluk chikamagluru distric 677126 kamalaka,india primary aim of the study is to evaluate the efficacy of gatuled panchange kwitha with serbased seetha which weit be most effective in managing symptoms of amlapitta in 30 days

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Subject of either sex.
  • Subject within the age group 18-60 yrs.
  • Subjects with clinical features of Amlapitta such as Avipaka, Klama, Uthklesha, Tikta Amlodgara, Gourava, Hruthkanta daha, and Aruchi will be included.
  • Subjects with controlled systemic disorder such as DM, HTN, etc will be included.
  • Subjects who are willing to give written consents for the study.

排除标准

  • Pregnant and Lactating women
  • Subjects with uncontrolled systemic disorder such as Diabetes mellitus, Hypertension, etc
  • Subject diagnosed with Gastro- intestinal disorders like peptic ulcer, pancreatic and hepatic disorders.
  • Subjects with history of haematemesis, malena and other systemic disorders that may interfere with the clinical trial.

结局指标

主要结局

Effect of treatment will be assessed on the basis of changes found in the gradation of the both individual and overall parameters according to their severity before, during and after treatment.

时间窗: 30 DAYS

SUBJECTIVE PARAMETERS

时间窗: 30 DAYS

Avipaka (digestion)

时间窗: 30 DAYS

Klama (tiredness)

时间窗: 30 DAYS

Uthklesha (nausea)

时间窗: 30 DAYS

Tikta amlodgara ( sour and bitter belching)

时间窗: 30 DAYS

Gourava (heaviness of body)

时间窗: 30 DAYS

Hruthkanta daha (burning sensation of throat )

时间窗: 30 DAYS

Aruchi (anorexia)

时间窗: 30 DAYS

次要结局

  • NOT APPLICABLE(NOT APLLICABLE)

研究者

发起方
Dr Vijayalakshmi Teggi
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Dr Vijayalakshmi Teggi

ALN Rao memorial Ayurvedic medical college

研究点 (1)

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