A Clinical Trial On Hyperacidity With Patolnimabadi Kashaya.

Open Label Single Arm Clinical Study To Evaluate the Effect Of Patolanimbadi Kashaya in Amlapitta. - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/04/065887

Enrollment

Registered

2024-04-18

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-29

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

Conditions

Health Condition 1: K929- Disease of digestive system, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Subjects having classical symptoms of Amlapitta Such As Avipaka ,Klama, Utklesh,Tikta-amlauadgar Hridakanthadaha, Aruchi, Gaurava. 2.Controlled cases of hypertension and diabetes mallitus 3.Chronicity not more than 1 year.

Exclusion criteria

Exclusion criteria: 1.Chronicity more than 1 year. 2.Known case of peptic ulcer,duodenal ulcer and Malignancy. 3.Symptoms like hematemesis and Malena. Pregnant and Lactating women.

Design outcomes

Primary

Measure	Time frame
To improve the quality of life in amlapitta patient.Timepoint: One month	—

Secondary

Measure	Time frame
To Reduce the Severity Of Amlapitta.Timepoint: 0th Day first Assessment 15th Day second Assessment 30th Day third Assessment 45th Day Final Follw up	—

Countries

India

Contacts

Public ContactDr Naiya Patel

G.J Patel Institute of Ayurvedic Studies and Research,new vallabh vidhyanagar ,Anand

soumya.ea@cvmu.edu.in9847003989

Outcome results