EVALUATION OF VACHA Acorus calamus IN THE MANAGEMENT OF AMLAPITTA HYPERACIDITY

CLINICAL EVALUATION OF VACHA Acorus calamus IN THE MANAGEMENT OF AMLAPITTA HYPERACIDITY - Nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/06/111768

Enrollment

Registered

2026-06-03

Start date

Unknown

Completion date

Unknown

Last updated

2026-06-22

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

Conditions

Health Condition 1: K929- Disease of digestive system, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients willing to fill written consent form to participate in research study Sex of either male or female Patients having cardinal symptoms of Amlapitta (hyperacidity)

Exclusion criteria

Exclusion criteria: Patients not willing to fill written consent form to participate in the research study Age below 21 years and above 60 years Chronicity more than 5 years Pregnant and lactating mothers Patients having diseases like gastric ulcers and duodenal ulcer etc Patients suffering from Amlapitta with any other chronic diseases like Asthama Malignancies Liver cirrhosis and Chronic renal failure Diabetes were excluded from the study

Design outcomes

Primary

Measure	Time frame
Avipaka (Indigestion) Utklesha (Nausea) Tikta-amla-udgar (Acidic regurgitation) Gourava (Heaviness) Hrit kanthadaha (Burning sensation) Aruchi (Anorexia) Timepoint: 30 days	—

Secondary

Measure	Time frame
nilTimepoint:	—

Countries

India

Contacts

Public ContactDr Urvashi Parte

Pt Khushilal Sharma Government Autonomus Ayurveda College and Institute Bhopal

deepika.smiling@gmail.com8143449578

Outcome results