An Interventional study to Manage Aruchi with Upavasa and Pachana.
Phase 2
- Conditions
- Health Condition 1: K929- Disease of digestive system, unspecified
- Registration Number
- CTRI/2024/07/071747
- Lead Sponsor
- Dr Sarita
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Male and Female patient having sign and symptoms of Aruchi
The individual between range 30-60 years and willing to give their informed written consent.
Exclusion Criteria
Pragnent and Lactating women
Patient having known Hypersensitivity
Patient below 30 and above 60 years
Patient having already diagnosed any associated chronic ailments like renal disorders alcoholic liver diseases and chronic hemolytic anaemia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction in scoring pattern of symptoms of Aruchi. <br/ ><br> <br/ ><br>Timepoint: 7th day <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method To estabilish the fact that Langhna upkarma (Upavasa and Pachana) have tremendrous effect on Aruchi : A rasa pradoshaj roga. <br/ ><br>Timepoint: Follow up visit to opd on 7th day