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Clinical Trials/CTRI/2025/03/082383
CTRI/2025/03/082383Not yet recruitingPhase 2

A comparative clinical study to evaluate the efficacy of Pathyadi churna in the management of Vidagdhajirna w.s.r to Hyperacidity.

Government Ayurvedic College and Hospital1 site in 1 country40 target enrollmentStarted: April 1, 2025Last updated:

Trial Snapshot

Phase
Phase 2
Status
Not yet recruiting
Sponsor
Enrollment
40
Locations
1
Primary Endpoint
Relief from sign and symptoms

Study Overview

Brief Summary

Vidagdhajirna is a disorder of a Annavaha Srotas characterized by Trishna (excessive thirst), Moha (unconsciousness), Bhram (giddiness), Amloudgar (sour eructation), Daha (Burning sensation). Now in present era, due to bad food habits and improper life style with world. 80% of the top ten life threatening diseases of the world are due to faulty dietary habits. Vidagdhajirna is similar to hyperacidity. Due to various factors in the progressive civilization of the present day like speedy environmental changes, adaptation of newer & newer food materials, change in method of cooking, atmospheric pollution, encroachment of various chemical agents in newer life styles, occupational hazards etc. have precipitated the increasing trend of the diseases. Along with those stimulating factors tremendous stress, strain, disturbed sleep & anxiety have significantly aggravated the diseases including Vidagdhajirna. This is a life style problem and those who are addicted to tobacco, alcohol as well as excess of packaged food with rich salt content use of spices and non-vegetarian food can be easily caught by this disease. The prevalence of hyperacidity in India ranges from 7.6% to 30%, being < 10% in most population studies, and higher in cohort studies.

Study Design

Study Type
Interventional
Allocation
Na
Masking
None

Eligibility Criteria

Ages
16.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • 1 Patients between the age group of 16 -60 yrs 2 Patients diagnosed as Vidagdhajirna according to Ayurvedic classical features like will be randomly selected irrespective of sex, religion and occupation.

Exclusion Criteria

  • 1 Lactating and pregnant women 2 Patient suffering from other systemic illness which may interfere with course of treatment.

Outcomes

Primary Outcomes

Relief from sign and symptoms

Time Frame: 30 days

Secondary Outcomes

  • Determination of effect of intervention w.r.t other(30 days)

Investigators

Sponsor
Government Ayurvedic College and Hospital
Sponsor Class
Other [Government Ayurvedic College and Hospital Budhamurti Kadamkuan Patna Bihar 800003 India]
Responsible Party
Principal Investigator
Principal Investigator

Dr Daisy Lal

Government Ayurvedic College and Hospital

Study Sites (1)

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