A COMPARATIVE CLINICAL STUDY TO EVALUATE THE EFFICACY OF PATOLADI KWATHA (Herbal decoction) AND PAARIBHADRADI KWATHA (Herbal decoction) IN THE MANAGEMENT OF AMLAPITTA (Hyper Acidity)

Phase 2

Not yet recruiting

• Conditions: Gastritis, unspecified,

• Registration Number: CTRI/2019/01/016977
• Lead Sponsor: DR NAGALAKSHMI A S

Brief Summary

AMLAPITTA IS ONE AMONG THE ANNAVAHA SROTO DUSHTI VIKARAS.THE LAKSANAS OF AMLAPITTA CAN BE CORRELATED WITHTHE SYMPTOMS OF HYPERACIDITY. HYPERACIDITY AFFECTS ABOUT 20% OF THE ADULTS WHOREPORT WEAKLY EPISODES OF HEARTBURN. THE PREVELANCE OF HEARTBURN AND OTHER ACIDREFLEX DISEASE ROSE NEARLY 50% OVER THE LAST DECADE. PATOLADI KWATHA WHICH ISMENTIONED IN CHAKRADATTA, AMLAPITTA CHIKITSA HAVING THE INGREDIENTS PATOLA,SHUNTI AND DHANYAKA HAS KAPHA PITTA HARA PROPERTY. PAARIBHADRADI KWATHAMENTIONED IN HARITHA SAMHITHA FOR AMLAPITTA CHIKITSA,WHICH HAS THE INGREDIENTSLIKE PAARIBHADRA DALA AND AMALAKI PHALA, PAARIBHADRA DALA WHICH HASPITTAROGAGHNA PROPERTY AND AMALAKI PHALA IS MADURA VIPAKA,WHICH IS BENEFICIALIN PITTAJA VIKARAS. THIS STUDY IS DOUBLE ARM OPEN LABEL COMPARATIVE CLINICALSTUDY COMPARING THE EFFICACY OF PATOLADI KWATHA 24ML TWICE DAILY FOR 14 DAYSAND PAARIBHADRADI KWATHA 24ML TWICE DAILY FOR 14 DAYS FOR 20 PATIENTS IN EACHGROUP WHICH INCULDES THE CLASSICAL SIGN & SYMPTOMS OF AMLAPITTA.THIS STUDYWILL BE CONDUCTED IN SRI KALABYRAVESHWARA SWAMY AYURVEDIC MEDICAL COLLEGEHOSPITAL AND RESEARCH CENTER, BENGALURU,KARNATAKA

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2019-07-01
• Study Start: 2019-10-01

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• Patients within the age group 20-70 years of either sex.
• Patients with samanya lakshanas of Amlapitta.

Exclusion Criteria

• Pregnant women and lactating mother .
• Complications which will intervene the course of treatment.
• Patients suffering from other systemic diseases which interfere with the course of treatment.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
EFFICACY OF INTERVENTION OVER SUBJECTIVE CRETIRIA OF AMLAPITTA.	14 days

Trial Locations

Locations (1)

Sri Kalabyraveshwara Swamy Ayurvedic Medical College Hospital and Research Centre; 🇮🇳 Bangalore, KARNATAKA, India

Sri Kalabyraveshwara Swamy Ayurvedic Medical College Hospital and Research Centre

🇮🇳Bangalore, KARNATAKA, India

Dr Rajashekhar C V

Principal investigator

8867212844

drrajhere@yahoo.co.in