Skip to main content
Clinical Trials/CTRI/2025/04/084669
CTRI/2025/04/084669Not yet recruitingPhase 3 4

Pharmacotherapeutic evaluation of Paribhadra Patra (Erythrina variegata Linn.) and Amlaki phala (Emblica officinalis Gaertn.) in the management of Amlapitta (Hyperacidity) - An exploratory study

PGIA DSRRAU Jodhpur1 site in 1 country30 target enrollmentStarted: February 6, 2025Last updated:

Trial Snapshot

Phase
Phase 3 4
Status
Not yet recruiting
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
Changes in the objective parameters

Study Overview

Brief Summary

My study titled "Pharmacotherapeutical Evaluation of Paribhadra Patra and Amalaki Phala in the Management of Amlapitta (Hyperacidity)" focuses on assessing the effectiveness of two traditional Ayurvedic remedies—Paribhadra Patra (leaves of Erythrina variegata) and Amalaki Phala (fruit of the Indian gooseberry)—in treating Amlapitta, commonly known as hyperacidity.

The research evaluates the pharmacological properties, therapeutic actions, and potential benefits of these remedies in alleviating symptoms such as indigestion, acidity, and gastritis. The study aims to provide scientific evidence supporting their use in managing hyperacidity and offers insights into their mechanisms of action, dosage, and safety profile in the context of Ayurvedic treatment practices.

Study Design

Study Type
Interventional
Allocation
Not Applicable
Masking
Open Label

Eligibility Criteria

Ages
16.00 Year(s) to 50.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Clinically and pathologically diagnosed patient , who are suffering from Amlapitta.

Exclusion Criteria

  • Subject should not suffering from Amlapitta more than 3 months
  • Age below 16 years and above 50 years
  • Subject reporting with complication like cardiac problem , emphysema, carcinoma etc.
  • will be excluded
  • Pregnant woman and lactating mothers was excluded
  • Subject with gastric malignancy
  • Subject who recently undergo gastro-intestinal surgery.

Outcomes

Primary Outcomes

Changes in the objective parameters

Time Frame: 1 month

Secondary Outcomes

  • Changes in the clinical sign and symptoms of Amlapitta(1 month)

Investigators

Sponsor
PGIA DSRRAU Jodhpur
Sponsor Class
Government medical college

Study Sites (1)

Loading locations...

Similar Trials