To Assess The Efficacy Of Jal Neti And Ushna Jal Paan In Vataja Pratishyaya.
- Conditions
- Health Condition 1: J309- Allergic rhinitis, unspecified
- Registration Number
- CTRI/2021/07/034804
- Lead Sponsor
- Department of Swasthavritta And Yoga
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.The patients with all general symptoms of Vataja Pratishyaya according to Ayurvedic texts.
2.Patients between the age group of 18 to 60 years.
3.Patients who give their consent in writing will be participating in this study.
1.Patient not willing to participate and did not gave written consent will be excluded.
2.Age of the Patients will be below 18 and above 60 years..
3.Patients with complications of this disease.
4.Those with any chronic debilitating infectious disease/ any inflammatory disease.
5.Those with requiring surgical treatment (e.g., for Nasal Polyp) .
6.Patient with history on any direct or indirect Trauma on nasal sinus.
7.Recent Nasal Surgery.
8.Patients who have Diabetic, Hypertension, Cardiac Pathology, Anemia, Immune Deficiency Disorders like AIDS, Tuberculosis, Pregnancy, Hepatic failure, Renal failure, Malignancy etc.
9.Patients restricted for particular Jal Neti and Ushna Jal Paan.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evaluation of decrease symptoms in Vataja Pratishyaya as follows, <br/ ><br>1.Nasa Srava ( Nasal discharge ) <br/ ><br>2.Kshavathu ( Sneezing ) <br/ ><br>3.Nasavarodha ( Nasal obstruction due to Kaph ) <br/ ><br>4.Shirahshoola ( Headache ) <br/ ><br>5.Swarabheda ( Change of voice ) <br/ ><br> <br/ ><br>Timepoint: the out come measures will be checked on day 0, 10, 20, 30 and Post study follow up 15 days
- Secondary Outcome Measures
Name Time Method Objective Parameters â?? <br/ ><br>1. Hematological examination :- CBC, AEC, RBS <br/ ><br>2. Nasal Peak Inspiratory Flow Rate ( NPIFR ) <br/ ><br>before and after intervention <br/ ><br>Timepoint: 30 days