A clinical study to evaluate the effectiveness of simhayadi kwatha and patoladipanchanga kwatha in the treatment of amlapitta (Gastro esophageal reflex disease)
Phase 2
- Conditions
- Health Condition 1: K219- Gastro-esophageal reflux disease without esophagitis
- Registration Number
- CTRI/2024/07/070382
- Lead Sponsor
- Dr Vijayalakshmi Teggi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Subject of either sex.
2. Subject within the age group 18-60 yrs.
3. Subjects with clinical features of Amlapitta such as Avipaka, Klama, Uthklesha, Tikta Amlodgara, Gourava, Hruthkanta daha, and Aruchi will be included.
4. Subjects with controlled systemic disorder such as DM, HTN, etc will be included.
5. Subjects who are willing to give written consents for the study.
Exclusion Criteria
1. Pregnant and Lactating women
2. Subjects with uncontrolled systemic disorder such as Diabetes mellitus, Hypertension, etc
3. Subject diagnosed with Gastro- intestinal disorders like peptic ulcer, pancreatic and hepatic disorders.
4. Subjects with history of haematemesis, malena and other systemic disorders that may interfere with the clinical trial.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Effect of treatment will be assessed on the basis of changes found in the gradation of the both individual and overall parameters according to their severity before, during and after treatment. <br/ ><br>SUBJECTIVE PARAMETERS <br/ ><br>Avipaka (digestion) <br/ ><br>Klama (tiredness) <br/ ><br>Uthklesha (nausea) <br/ ><br>Tikta amlodgara ( sour and bitter belching) <br/ ><br>Gourava (heaviness of body) <br/ ><br>Hruthkanta daha (burning sensation of throat ) <br/ ><br>Aruchi (anorexia)Timepoint: 30 DAYS
- Secondary Outcome Measures
Name Time Method OT APPLICABLETimepoint: NOT APLLICABLE