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Study on Guduchyadi Gana to see the effect in patients having symptoms related to Ama which are explained in classical text Ashtanga Hridaya

Phase 2
Not yet recruiting
Conditions
Disease of stomach and duodenum, unspecified. Ayurveda Condition: AMADOSHAH,
Registration Number
CTRI/2025/03/082180
Lead Sponsor
Institute of Teaching and Research in Ayurveda
Brief Summary

The study aims to access the effect of guduchyadi gana in the form of Ghanavati in the patients having ama lakshana. Participants will be asked questions from IEC approved  questionnaire for Ama Lakshana maid by Dr Suresh Panchal MD scholar of RNVV department ITRA, Jamnagar. If participants shows minimum 4 sign or symptoms of Ama mentioned in Ashtanga Hridaya sutra sthana 13th Adhyaya will be enrolled in the study .Total 100 participants will be enroll in study and will be divided into two groups 50 participants each. One group i.e. trail group will receive Guduchyadi Ghanavati with dose of 500mg 2 Ghanavati in Pragbhakta Kala with Ushnodaka for 15 days. Other group will receive placebo in the form of roasted suji capsules with dose of 500mg 2 capsules in Pragbhakta Kala with Ushnodaka for 15 days. As there is no data available of other drug or formulation showing similar properties as Guduchyadi Gana placebo in the form of Roasted suji capsules are chose to compare trail drug. Both the groups will receive same pathya apathya chart and will be counselled about it. The results will be assessed and end of treatment and  improvement or modifications related to Ama Lakshana will be assessed using same questionnaire. Results and discussion will done based on data collected.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
100
Inclusion Criteria
  • 1.Patients having minimum 4 signs or symptoms of Ama.
  • 2.The patients diagnosed with other disease having sign or symptoms of Ama will be included in the study.
  • 3.Age between 18 to 50 years.
  • 4.Chronicity less than 3 months.
Exclusion Criteria
  • 1.Age less than 18 years and more than 50 years.
  • 2.Patients suffering from any other disease which intervenes with the treatment.
  • 3.Patients having major systemic disease like cardiac disease, ulcerative colitis, chronic kidney disease, diabetes mellitus, hypertension, thyroid disorders etc.
  • 4.Pregnant women and Lactating mothers.
  • 5.Patients taking the course of any allopathic or other medicine.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Modification in subjective criteria in the form of questionnaire with answer in grades like 0,1,2,3 of Ama Lakshana according to severityassess after 15 days of course
Secondary Outcome Measures
NameTimeMethod
1.Improvment in the clinical condition of Ama Lakshana.2.Improvment in the quality of Life.

Trial Locations

Locations (1)

PG hospital Institute of teaching and research in ayurveda Jamnagar Gujrat

🇮🇳

Jamnagar, GUJARAT, India

PG hospital Institute of teaching and research in ayurveda Jamnagar Gujrat
🇮🇳Jamnagar, GUJARAT, India
Dr Pallavi Janardhan Buddhe
Principal investigator
09284049979
buddhepallavi@gmail.com

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