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EFFECT OF GUDUCHYADICHURNA AND ELADICHURNA IN AMLAPITTA(HYPERACIDITY)

A CLINICAL STUDY OF GUDUCHYADICHURNA AND ELADI CHURNA IN THE MANAGEMENT OF AMLAPITTA

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/05/008719
Enrollment
30
Registered
2017-05-31
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- PATIENT SUFFERING FROM AMLAPITTA.

Interventions

Intervention1: A CLINICAL STUDY OF GUDUCHYADICHURNA IN THE MANAGEMENT OF AMLAPITTA: 15 patients will be taken in group A and will be treated with Guduchyadi churna in following dose and duration Dose

Sponsors

GOVT AKHANDANAND AYURVED COLLEGE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with classical signs & symptoms of Amlapitta.Avipaka (Indigestion), Klama(Lassitude), Utklesha (Nausea), Tiktodgara(Bitter eruction), Amlodgara(sour eruction),Gaurav(heaviness of body),Hrit Daha(Heart buru), Kantha Daha (Burning in throat), Aruchi (Anorexia).

Exclusion criteria

Exclusion criteria: Patients suffering from Hematemesis, Acute diarrhoea, Intestinal T.B, Gastric and Peptic ulcer, uncontrolled D.M. and HTN, Arsha, Carcinoma, cardiac disorders etc. serious condition of the patient.

Design outcomes

Primary

MeasureTime frame
Result will be assessed on the basis of relief in the Signs and symptoms of AmlapittaTimepoint: 4 WEEKS—

Secondary

MeasureTime frame
Result will be assessed on the basis of relief in the Signs and symptoms of AmlapittaTimepoint: 4 weeks—

Countries

India

Contacts

Public ContactMOHIT PRAVINBHAI PAGHDAR

GOVT AKHANDANAND AYURVED COLLEGE BHADRA AHMEDABAD

patanjaliayucare@yahoo.com9426336822

Outcome results

None listed

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