To see the effect of Lavangadi decoction in indigestion.

A SINGLE ARM CLINICAL STUDY TO EVALUATE THE EFFICACY OF LAVANGADI KASHAYA IN AJEERNA

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/01/039195

Enrollment

Registered

2022-01-06

Start date

Unknown

Completion date

Unknown

Last updated

2022-02-21

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)Patient with sign and symptoms Glani, Gaurav, Vishtambha, Bhrama, Marutamudhata, Ati mala pravrutti as mentioned in Yog Ratnakar. (minimum 2 symptoms present will be included) 2)Selection of patients will be irrespective of gender and socio-economical class. 3)Age limit from 18- 60 yrs. 4)Patients who are willing to enroll in the research.

Exclusion criteria

Exclusion criteria: 1)Oesophageal Varices. 2)Chronic liver diseases. 3)Cancer of Oesophagus, Stomach. 4)Gastric ulcers, Duodenal ulcers. 5)Chronic illness and infection like Tuberculosis, Cancer(malignancy). 6)Pregnant women / Lactating mothers.

Design outcomes

Primary

Measure	Time frame
Clinical study of Lavangadi Kashaya in Udargourav due to Ajeerna.Timepoint: 14 Days study with two follow ups (0, 7, 14th day)	—

Secondary

Measure	Time frame
a) To treat Agnimandya. b) To assess present day lifestyle and diet as a causative factor for Ajeerna. Timepoint: 14 Days study with two follow ups (0, 7, 14th day)	—

Countries

India

Contacts

Public ContactShreya Bhatia

Dr D Y Patil College Of Ayurveda And Research Center

gunvantayurved@gmail.com9028321955

Outcome results