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effect of Vaarisara dhouti procedure and Kamadudha rasa medicine in Amlapitta

A Controlled Clinical Trial to Evaluate the Effect of Vaarisara Dhouti in the Management of Amlapitta - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067770
Enrollment
30
Registered
2024-05-21
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: K00-K95- Diseases of the digestive system

Interventions

None listed

Sponsors

KSGDEWFs Sanjeevini Ayurveda Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of Amlapitta within the age of 18 - 50 years of either sex, having the symptoms of Amlapitta like Avipaka, klama, Tikta-Amla udgara and Hrit-Kanthadaha since 3 months and consenting to participate in the study will be included.

Exclusion criteria

Exclusion criteria: Pregnant and lactating woman. Patients with complaints of hemoptysis, anal bleeding Patients of duodenal, peptic ulcers, Hernia, piles and fissure etc Patients who have undergone any recent surgeries. Patients with severe systemic disorders.

Design outcomes

Primary

MeasureTime frame
vaarisara dhouti will reduce recurrence of AmlapittaTimepoint: on 7days ofpractice—

Secondary

MeasureTime frame
reduction in recurrenceTimepoint: 7 days—

Countries

India

Contacts

Public ContactDr Amrutha Kalyani

RGUHS

amrutha.kalyani@gmail.com7406559247

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026