EUCTR2006-001837-16-IT进行中（未招募）不适用
PRULIFLOXACIN VERSUS LEVOFLOXACIN IN PATIENTS WITH ACUTE BACTERIAL RHINOSINUSITIS ABRS - ND
ANGELINI0 个研究点目标入组 284 人开始时间: 2006年6月23日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 284
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •MALE OR FEMALE ADULTS WITH NO LIMITATION OF RACE; ABRS DEFINED AS A VIRAL UPPER RESPIRATORY TRACT INFECTION CHARACTERIZED BY INCREASE OF SYMPTOMS AFTER 5 DAYS, OR PERSISTENT SYMPTOMS FOR 10 DAYS BEFORE THE SCREENING VISIT, WITH LESS THAN 12 WEEKS DURATION; CLINICAL DIAGNOSIS OF ABRS CHARACTERIZED BY THE PRESENCE OF TWO OR MORE OF NASAL BLOCKAGE/CONGESTION, DISCHARGE ANTERIOR/POST NASAL DRIP, FACIAL PAIN/PRESSURE, REDUCTION/LOSS OF SMELL; CLINICAL DIAGNOSIS OF MODERATE/SEVERE ABRS; WRITTEN INFORMED CONSENT
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •HYPERSENSITIVITY OR ALLERGY TO FLUOROQUINOLONE ANTIBACTERIALS AND/OR TO ANY COMPONENT, NOSOCOMIAL SINUS INFECTION OR INFECTIONS FOLLOWING OR ASSOCIATED WITH NASO-TRACHEAL INTUBATION, CHRONIC OR COMPLICATED RHINOSINUSITIS, NASAL POLYPS, HISTORY OF SINUS SURGERY.
研究者
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