Study of effect of Guduchyadi decoction in acidity.

Comparative Prospective Phase II Clinical Study to Evaluate the Efficacy of Guduchyadi Kwatha in Urdhvaga Amlapitta. - nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2020/09/027968

Enrollment

Registered

2020-09-22

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: K928- Other specified diseases of the digestive system

Interventions

Intervention1: Guduchyadi Kwatha: Orally 40 ml two times a day before meal with honey for 21 days Control Intervention1: Bhunimbadi Kwatha: 40 ml two times a day before meal with honey for 21 days

Eligibility

Inclusion criteria

Inclusion criteria: patients having symptoms of urdhvag amlapitta patients willing for trial and giving consent patient from all socio economic status

Exclusion criteria

Exclusion criteria: pregnent and lactating women patients having hepatic disorders and other complications patient suffering from any infectious diseases patient suffering from major illness

Design outcomes

Primary

Measure	Time frame
chest burning reduced vomiting reduced abdominal pain reducedTimepoint: 21 days	—

Secondary

Measure	Time frame
Hyperacidity ReducedTimepoint: 21 days	—

Countries

India

Contacts

Public ContactDr Rajan Balwant Kulkarni

Ayurved sevha sangha Ayurved mahavidyalaya nashik

vaidyarajankulkarni@gmail.com9823350440

Outcome results

None listed

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