A comparative clinical intervention to evaluate the main outcome of purgation followed by patoladi decoction and patoladi decoction in Gastritis

An open label randomised comparative clinical study to evaluate the efficacy of virechana followed by patoladi kwatha and patoladi kwatha in amlapitta - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/08/071941

Enrollment

Registered

2024-08-06

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

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

Conditions

Health Condition 1: K297- Gastritis, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1 Subjects with Samanya Lakshanas of Amlapitta 2 Subjects between age group of 18to 60 years of either gender 3 Subjects who are fit for Virechana karma

Exclusion criteria

Exclusion criteria: 1 Subjects suffering from other systemic illness which interfere the course of study 2 Pregnant and Lactating women with features of Amlapitta

Design outcomes

Primary

Measure	Time frame
To see the therapeutic effect and prolonged sustainence of Patoladi kwatha and Sodhana Purvaka Patoladi kwatha in AmlapittaTimepoint: Before intervention baseline After intervention 30 days and after follow up 45 days	—

Secondary

Measure	Time frame
nilTimepoint: nil	—

Countries

India

Contacts

Public ContactVijayalakshmi s

Sri Kalabyraveshwara Swamy Ayurvedic Medical College Hospital and Research Centre

drviju.prati.09@gmail.com9964815059

Outcome results