CTRI/2012/03/002478招募中4 期
Evaluation of the effect of combination of moxifloxacin and voriconazole on QT interval of healthy volunteer and renal failure patients
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 入组人数
- 16
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
- •Healthy volunteers who gives consent to participate in the study
- •Renal failure patients whose creatinine clearance is 10-50 ml/min
排除标准
- •Baseline QTC interval >450millisec on 3 repeated occasions
- •Use of concomitant medication that prolong QT interval
- •Use of any drug that inhibit or induce CYP450 enzymes and/or P-gp within 30 days prior to screening
- •family history of congenital long QT syndrome (LQTS) or sudden death
- •known allergic or contraindication to voriconazole or moxifloxacin
- •Pregnant or lactating mother
- •HIV positive patient
- •HBsAg positive individuals
- •Alcoholics and
- •Presence of significant cardiovascular, pulmonary, hepatic, renal, haematological, gastrointestinal, endocrine, immunologic, dermatologic, neurological, or psychiatric disease
研究者
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