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A Clinical Study Of Vaman Karma (Vomiting Process) In The Management Of Urdhvag Amlapitta (Hyper Acidity)

A Clinical Study Of Vaman Karma In The Management Of Urdhvag Amlapitta.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/06/006995
Enrollment
30
Registered
2016-06-06
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Patients Of Urdhvag Amlapitta

Interventions

Intervention1: Vaman Karma followed By Shaman: By Vatsak Beej - 6-8gm Shaman by Phaltrikadi Ghanvati-6gm tds & duration-6 weeks MOA : Orally Control Intervention1: Shaman: Phaltrikadi Ghanvati Dose-6

Sponsors

Goverment Akhandanand Ayurveda College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The Patients will be selected on the basis of sign & symptoms of Urdhvag Amlapitta Described in Ayurveda Classics From Akhandanand Ayurveda College & Maniben Ayurveda College Ahmedabad

Exclusion criteria

Exclusion criteria: Vaman Ayogya,Haemetemesis,Acute diarrhoea, Intestinal T.B,Gastric & Peptic Ulcer,DM,HT,Gulma,Atisar,Arsha,Cancer,AIDS,Heart Disease

Design outcomes

Primary

MeasureTime frame
All signs & symptoms of Amlapitta will be asigned score depending upon is their severity to assess of effect of drug.Timepoint: 1 year—

Secondary

MeasureTime frame
NilTimepoint: Nil—

Countries

India

Contacts

Public ContactArchi Ajitkumar Desai

Government Akhandanand Ayurveda college,Bhadra,Ahmedabad-1

ram.ayu@gmail.com9925505758

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026