To compare efficacy of kokilakshadi kashayam & kaishore gugguluin management of vatarakra wsr to gout
- Conditions
- Health Condition 1: E790- Hyperuricemia without signs of inflammatory arthritis and tophaceous disease
- Registration Number
- CTRI/2023/07/055000
- Lead Sponsor
- Shri krishna government ayurvedic college and hospital sec 8 umri road kurukshetra
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Patients between the age group of 19-60 years of either sex presented with clinical features of VataRakta/ Gout.
2.Diagnosed and confirmed the case of VataRakta (Gout).
3.Patients have serum uric acid levels of more than 6mg/dl in females & more than 7mg/dl in males with or without any associated features like joint pain and inflammation.
1.Patients below 19 years and above 60 years will be excluded
2.Patients suffering from other forms of Arthritis like Rheumatoid arthritis, Osteoarthritis, Ankylosing spondylitis, Infective arthritis, etc.
3.Pregnant and lactating mother.
4.Subject showing the uric acid level above 9mg/dl.
5.Patients with evidence of malignancy & on chemotherapy drugs.
6.Patients having any disorders like Diabetes mellitus, Cardiac disease, CRF, ARF, etc.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The efficacy of Kokilakshadi Kashayam and Kaishore Guggulu will be noted in respective groups as per changes in subjective criteria on the 15th 30th day and 60th-day post-treatment and repeat lab investigation (CBC, ESR, CRP (Quantitative), Serum UA, Blood Urea, Serum Creatinine, RA Factor) will be done post-treatment.Timepoint: 30 days of treatment with follow up on 15th, 30th and 60th day
- Secondary Outcome Measures
Name Time Method 1) To Compare efficacy of Kokilakshadi Kashaya & Kaishore Guggulu after complete treatment & follow up of both groups. <br/ ><br>2.Evalution of adverse effect of both drug will be done on each patient during & post treatment.Timepoint: Final result will be checked post treatment of all patients from both groups & will take approx 1 year <br/ ><br>2) Adverse effects will be noted on each patient & each follow up till 60th day