CTRI/2017/12/010914尚未招募3 期
A Randomized, Open label, Comparative Clinical Study to Evaluate the Efficacy and Safety of Cystone Forte Tablet in Urolithiasis
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
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
- •Subject with Urolithiasis as diagnosed by clinical with calculi measuring 5 to 12 mm.
- •Hematologic and Biochemical parameters within normal limits (Study specific parameters: calcium, uric acid cannot be more than 2 times upper limit of normal value).Willing to sign inform consent document.
排除标准
- •Subjects with severe obstructive uropathy,those with serious systemic medical disorder- Hypertension, Severe Diabetes, Metabolic disorders, Endocrinal disorders, cardiac illness,the subjects not to have used any drugs, for at least 1 week prior to the study for concurrent illness with diabetes and Hypertension.
- •Subjects with a strong history of food or drug allergy of any kind,Subjects not to have been on weight reducing diets within 3 months prior to the start of the study.Pregnant and lactating women
- •Patients unwilling to provide informed consent or abide by the requirements of the study.
研究者
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