Management of Acidity with kunjal kriya and Eladi churna

A COMPARATIVE CLINICAL STUDY TO EVALUATE THE EFFICACY OF ELADI CHURNA AND KUNJAL KRIYA IN AMLAPITTA W.S.R TO HYPERACIDITY - Amlapitta and Hyperacidity

Status

Active, not recruiting

Phases

Phase 1Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/04/107443

Enrollment

Registered

2026-04-02

Start date

Unknown

Completion date

Unknown

Last updated

2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K219- Gastro-esophageal reflux disease without esophagitis

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either gender and between 18-60 years of age. 2. Patients willing and able to carry out treatment for 6 weeks. 3. Patients will be registered with duly signed informed consent prior to the trail.

Exclusion criteria

Exclusion criteria: 1. Patients with diagnosed cases of gastric, peptic and duodenal ulcers. 2. Patients with any GIT, abdominal complications and chronic illness. 3. Patients with diagnosed cases of any systemic disorder. 4.Pregnant and lactating women.

Design outcomes

Primary

Measure	Time frame
The study will evaluate the clinical efficacy of Eladi churna and kunjal kriya in Amlapitta and provide scientific evidence for their role in improving Hyperacidity and quality of lifeTimepoint: 6 month	—

Secondary

Measure	Time frame
The study will evaluate the clinical efficacy of Eladi churna and kunjal kriya in Amlapitta and provide scientific evidence for their role in improving Hyperacidity and symptoms such as indigestion, tiredness, nausea, vomiting, bitter and acidic vomiting.Timepoint: 6 month	—

Countries

India

Contacts

Public ContactDr Sudesh Kumar Bhambu

Sri ganganagar college of ayurvedic science and hospital, Tantia University, Rajasthan 335002

drskb07@gmail.com919468709698

Outcome results