EFFECT OF GUDUCHYADICHURNA AND ELADICHURNA IN AMLAPITTA(HYPERACIDITY)

Recruiting

• Conditions: PATIENT SUFFERING FROM AMLAPITTA.

• Registration Number: CTRI/2017/05/008719
• Lead Sponsor: GOVT AKHANDANAND AYURVED COLLEGE

Brief Summary

**This study is a randomised, participants blinded, parallel group, active controlled trial to evaluate the efficacy of *Guduchyadi Churna in a*Dose of  10gm/day two divided dose with water Duration: 4 weeks in 15 patients with GROUP A and also  to evaluate the efficacy of  *Eladi Churna in a*Dose of  10gm/day two divided dose with water Duration: 4 weeks in 15 patients of GROUP B in Amlapitta.**

Detailed Description

Not available

Study Timeline

• Study Start: 2017-05-23
• Last Update Posted: 2017-05-31

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: All
• Target Recruitment: 30

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

• 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.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Result will be assessed on the basis of relief in the Signs and symptoms of Amlapitta	4 WEEKS

Secondary Outcome Measures

Name	Time	Method
Result will be assessed on the basis of relief in the Signs and symptoms of Amlapitta	4 weeks

Trial Locations

Locations (1)

AKHANDANAND AYURVED COLLEGE; 🇮🇳 Ahmadabad, GUJARAT, India

AKHANDANAND AYURVED COLLEGE

🇮🇳Ahmadabad, GUJARAT, India

DR MOHIT PAGHDAR

Principal investigator

8866608559

dr.mppaghdar273@gmail.com