To Study the Effect of Guduchyadi kwatha in the management of Dyspepsia in adults age of 18-60 years for a period of 30days.

A Controlled Clinical Study on the Efficacy of Guduchyadi Kwatha in the Management of Amlapitta. - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/06/069458

Enrollment

Registered

2024-06-25

Start date

Unknown

Completion date

Unknown

Last updated

2024-07-22

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

Conditions

Health Condition 1: K30- Functional dyspepsia

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Participants selected on the basis of presence of classical symptoms of Amlapitta. 2.Participants of either sex and of age group between 18 - 60yrs.

Exclusion criteria

Exclusion criteria: 1.Participants age less than 18years and above 60years. 2.Participants with GERD, Gastric or Duodenal ulcer and Malignancy of Stomach. 3.Participants with alarming features of dyspepsia like Weight loss, Anaemia, Haemetemsis and Dysphagia. 4.Participants with drug induced uncontrolled Diabetes Mellitus and uncontrolled Hypertension. 5.Pregnant and Lactating women.

Design outcomes

Primary

Measure	Time frame
Improvements noticed in reduction in signs and symptoms based on •Global overall symptom scale •Quality of life in Reflux and Dyspepsia Questionnaire Timepoint: 0th day, 15th day, 30th day, after trial 45th day	—

Secondary

Measure	Time frame
Improvements noticed based on quality of life and reduction in signs and symptoms of Amlapitta.Timepoint: 0th day, 15th day, 30th day, after trial 45th day	—

Countries

India

Contacts

Public ContactDr M K N Anusha

Shri Dharmasthala Manjunatheshwara Institute of Ayurveda and Hospital Bengaluru

ssomayaji78@gmail.com9448211053

Outcome results