None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patient with appropriate symptoms of upper abdominal pain nausea waterbrash headache flatulence excessive sweating loss of body weight lack of food intake Patient who are willing to sign consent form and undergo laboratory investigations
Exclusion criteria
Exclusion criteria: Pregnant and lactating women Haemetemesis Malena Pancreatitis Inflammatory bowel disease Hyertensive heart disease Chronic kidney disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The therapeutic efficacy of trial drug Uppu Chenduram II on Eri GunmamTimepoint: 30 days | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of Siddha diagnostic parametersTimepoint: 30 days | — |
Countries
India
Contacts
Government Siddha Medical college and hospital