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Comparison of Dhatri-chatussamaavaleha and Abhayadi leha in Urdhwag Amlapitta(Hyperacidity).

A randomised comparative clinical trial to evaluate the efficacy of Dhatri-chatussamaavaleha with Abhayadi leha in Urdhwag Amlapitta.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/02/023265
Enrollment
62
Registered
2020-02-11
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: K293- Chronic superficial gastritis

Interventions

Intervention1: Dhatri-chatussamaavaleha: Group A will be treated with Dhatri-chatussamaavaleha containing Amalaki,Shatavari, Madhu and Sharkara.Dhatri-chatussamaavaleha will be given orally in the dos

Sponsors

PDEAs College of Ayurved and Research centre Nigadi Pune
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who are having six or more following signs and symptoms 1.Chhardi (Vomiting) 2.Amlodgar (Flatulence) 3.Hrullas (nausea) 4.Hruda-kantha daha (Burning sensation in chest-throat) 5.Udardaha (Burning sensation in the stomach) 6.Shirashool (headache) 7.Hastapada daha (Burning sensation in foot and hands) 8.Aruchi (Loss of appetite) 9.Mandalotpatti (urticarial rash)

Exclusion criteria

Exclusion criteria: 1.The known case of Gastric ulcer, duodenal ulcer, Stomach cancer, cancer of esophagus, esophageal varices, hematemesis. 2.Patients with long term use of steroids and pain killers. 3.Sever malnourished patients. 4.Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
To compare the efficacy of Dhatri-chatussamaavaleha 1 gm twice a day before meal with Ghee mixed Milk with Abhayadi leha 1 gm twice a day before meal with Honey in Urdhwag Amlapitta within 21 days.Timepoint: 21 days with follow up on 7th, 14th, and 21 st day.

Secondary

MeasureTime frame
1.To compare and study the efficacy of Dhatri-chatussamaavaleha. 2.To compare and study the efficacy of Abhayadi leha. 3.To study the adverse effect if any.Timepoint: 21 days with follow up on 7th, 14th, and 21 st day.

Countries

India

Contacts

Public ContactDr Snehal Chandrakant Ranzunjare

PDEAs College of Ayurved and Research Centre Nigadi Pune

khobragaderupali19@gmail.com8378929859

Outcome results

None listed

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