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Effect of Vamana Virechana and Pippalikhanda in Amlapitta or Hyperacidity

Efficacy of Vamana and Virechana Karma along with Pippalikhanda in the management of Amlapitta w.s.r. to Hyperacidity: an open labelled randomized comparative clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/12/010915
Enrollment
30
Registered
2017-12-19
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Patient diagnosed with Amlapitta

Interventions

Intervention1: Vamana with Madanphaladi Yoga followed by Pippalikhanda for 30 days: In Group A Patient will undergo Deepana Pachana with Musta and Shunthi churna 2-3 gms TDS for 3-7 days followed by S

Sponsors

Institute for Post Graduate Training And Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with all forms of Amlapitta who are clinically fit to undergo Virechana and Vamana. 2. Patient presenting with pratyatm lakshan of Amlapitta like Utklesha (Nausea), Hriddaha (Heart Burn), Kanthadaha (Burning sensation in throat), Amlodgara (Acid eruption), Vanti (Vomiting), Udara shoola (Pain in abdomen) with and without other pratyatm lakshan like Aruchi Adhmana etc. 3. Patients of either sex between 18-60 year ages.

Exclusion criteria

Exclusion criteria: 1. Patients below 18 year and above 60 years of ages. 2. Patients who are clinically unfit for Vamana and Virechana karma. 3. Subject suffering from acute gastrointestinal disorders like: a) Peptic ulcer b) Duodenal ulcer c) Pancreatic and hepatic disease d) Motility disorder e) Inflammatory bowel disease 4. Lactating and pregnant women 5. Any other severe complicating systemic illness 6. Patients who are not willing to be included in the study.

Design outcomes

Primary

MeasureTime frame
Relief in sign and symptoms of AmlapittaTimepoint: 6 weeks

Secondary

MeasureTime frame
Improves quality of life of the personTimepoint: 6 weeks

Countries

India

Contacts

Public ContactProf Anup B Thakar

Institute for Post Graduate Training And Research Centre

anup_thakar@yahoo.com9427776660

Outcome results

None listed

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