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Effect of Aragvadhamrutadi Kashaya vs patoladi kashaya in Amlapitta

Randomised Controlled Clinical Trial to Determine Efficacy of Aragvadhamrutadi Kashaya in Management of Amlapitta w.s.r.to Non-Ulcer Dyspepsia - Nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092964
Enrollment
80
Registered
2025-08-13
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Intervention1: To compare the efficacy of Aragvadhamrutadi Kashaya and patoladi kwath in management of Amlapitta: 18 Months Intervention2: Aragvadhamrutadi Kashaya: group A patients given 40ml of Arag

Sponsors

SST Ayurved Mahavidyalaya Sangamner
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 All the patients with sign and symptoms of Amlapitta like Avipak, Klama(Tiredness), Utklesh(Nausea), Tikta-amla Udgar(Bitter-sour belching), Gaurava(Abdominal heaviness), Hrud-Kanth Daha, Aruchi. 2 Patients who are ready to sign inform consent form. 3 patients with age group 18 to 50 years irrespective of sex.

Exclusion criteria

Exclusion criteria: 1 Known case of bleeding disorders, CA stomach patients. 2 Known case of severe systemic disorder and endocrine disorder like DM, Thyroid disorder patients. 3 Lactating and pregnant women. 4. Known case of TB, HIV, Hiatus-hernia, achalasia cardia. 5. Known case of Helicobacter Pylori infection.

Design outcomes

Primary

MeasureTime frame
Randomized controlled clinical trial to determine efficacy of Aragvadhamrutadi Kashaya in management of Amlapitta w.s.r. to Non- Ulcer Dyspepsia.Timepoint: 18 Months

Secondary

MeasureTime frame
relief of amlapitta symptomsTimepoint: 4 weeks

Countries

India

Contacts

Public ContactSavita Potalaji Kamle

SSTs Ayurved Mahavidyalaya ,Sangamner

kamlesp93@gmail.com8999718685

Outcome results

None listed

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