CTRI/2017/11/010615已完成2 期
Add on effect of Shunthi Gokshura Kwath over Amavatari Rasa in Amavata with special reference to Rheumatoid Arthritis â?? A Randomised open clinical trial.
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 64
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1. Patients having classical features of Amavata (Angamarda, Aruchi, Trishna, Alasya, Gaurava, Jwara, Apaka, Shoonata anganam)
- •2. Patients having the Pratyatma lakshana of Amavata (Shotha, Sandhi ruja, Sandhi graha, Sarwanga / Ekanga Sandhi Sotha, Arati)
- •3. Pravriddha Lakshana of Amavata (Agni daurbalya, Praseka, Aruchi, Gaurava, Vairasya, Ruja and Shotha in Hasta, Pada, Shiro, Gulpha, Trika, Janu, Uru Sandhi, Vrishchika Danshavat Vedana, Kukshi kathinya, Kukshi shula, Vibandha, Anaha, Hritgraha, Antra kujana, Chhardi, Jadya, Bhrama, Murchcha, Nidra-Viparyaya, Daha, Bahumutrata)
- •4. ARA Criteria - Patients who have at least one joint with definite clinical synovitis (swelling) with the synovitis not better explained by another disease
排除标准
- •1. Patients with other systemic complications of RA like RHD, Rheumatic fever, pleural â?? pericardial disease. Patients with poorly controlled Hypertension ( >160/100 mm of Hg)
- •2. Patients with Diabetes Mellitus (Fasting blood sugar more than 126 mg% and / or Post Prandial blood sugar more than 200 mg% OR HbA1c > 6.5%}
- •3. Patients diagnosed with other arthritis like gouty arthritis, tuberculous arthritis etc.
- •4. Patients who are unable to walk without support and / or confined to wheel chair.
- •5. Patients on prolonged ( > 6 weeks) medication with corticosteroids, antidepressants, anticholinergic, etc. or any other drugs that may have an influence on the outcome of the study
- •6. Patients who have a past history of Atrial Fibrillation, Acute Coronary Syndrome, Myocardial Infarction, Stroke or Severe Arrhythmia in the last 6 months.
- •7. Patients with concurrent serious hepatic disorder (defined as Aspartate Amino Transferase (AST) and / or Alanine Amino Transferase (ALT), Total Bilirubin, Alkaline Phosphatase (ALP) > 2 times upper normal limit) or Renal Disorders (defined as Creatinine >1.2mg/Dl), Severe Pulmonary Dysfunction (uncontrolled Bronchial Asthma and / or Chronic Obstructive Pulmonary Disease [COPD]), or any other condition that may jeopardize the study.
- •8. Alcoholics and/or drug abusers.
- •9. H/o hypersensitivity to any of the trial drugs or their ingredients.
- •10. Pregnant / lactating woman.
- •11. Patients who have completed participation in any other clinical trial during the past 6 months.
研究者
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