A CLINICAL STUDY OF AMLAPITTA WITH DRAKSHADI VATI AND PATOLADI GHANVATI

Not yet recruiting

• Conditions: AMLAPITTA (HYPER ACIDITY)

• Registration Number: CTRI/2018/07/015068
• Lead Sponsor: GOVERNMENT AKHANDANAND AYURVED MAHAVIDHYALAYA

Brief Summary

AIM OF THIS STUDY IS TO KNOW EFFICACY OF AMLAPITTA IN TRIAL GROUP. THIS STUDY IS RANDOMISED, PATIENTS SELECTION IS BLINDED. DRAKSHADI VATI AND PATOLADI GHANVATI WILL BE GIVEN AS PER TEXT.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2018-07-26
• Study Start: 2018-07-30

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• (2)Patients with classical signs & symptoms of Urdhvag Amlapitta.
• Avipaka (Indigestion), Klama(Lassitude),Utklesha (Nausea), Tiktodgara(Bitter eruction),Amlodgara(sour eruction), Gaurav(heaviness of body), HritDaha (Heart burn), KanthaDaha (Burning in throat),Aruchi (Anorexia).

Exclusion Criteria

• (1)Patients having age < 18 years and > 60 years.
• (2)Patients suffering from Hematemesis, Acute diarrhea, 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
ALL THE SIGN AND SYMPTOMS OF AMLAPITTA WILL BE ASSIGNED SCORE DEPENDING UPON THEIR SEVERITY TO ASSESS THE EFFECT OF THE DRUGS AT THE TIME OF BEFORE AND AFTER TREATMENT	4 WEEKS

Secondary Outcome Measures

Name	Time	Method
ALL THE SIGN AND SYMPTOMS OF AMLAPITTA WILL BE ASSIGNED SCORE DEPENDING UPON THEIR SEVERITY TO ASSESS THE EFFECT OF THE DRUGS AT THE TIME OF BEFORE AND AFTER TREATMENT	4 WEEKS

Trial Locations

Locations (1)

Akhandanad Ayurveda Collage Bhadra Ahmedabad; 🇮🇳 Ahmadabad, GUJARAT, India

Akhandanad Ayurveda Collage Bhadra Ahmedabad

🇮🇳Ahmadabad, GUJARAT, India

Dr JAYANTI PRAJAPATI

Principal investigator

9925799795

drjayprajapati93@gmail.com