跳至主要内容
临床试验/EUCTR2004-001460-42-DE
EUCTR2004-001460-42-DE进行中(未招募)不适用

A prospective, randomized, open-label, active-controlled study in adult subjects with acute bacterial sinusitis comparing the clinical efficacy of telithromycin (KETEK®) 800 mg once a day for 5 days versus amoxicillin-clavulanic acid (AUGMENTIN®) 875/125 mg twice a day for 10 days.

Aventis Intercontinental - Sanofi-aventis0 个研究点目标入组 298 人开始时间: 2004年9月16日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
298

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

  • Clinical diagnosis of ABS (signs and symptoms lasting longer than 7 days and less than 28 days, purulent anterior or posterior nasal discharge, one additional major sign and symptom or two minor signs and symptoms.
  • The major and minor signs and symptoms will be defined as the following: Major signs and symptoms: facial pain / pressure / tightness over the maxillary sinuses, nasal congestion / obstruction, change in the perception of smell (hypoanosmia / anosmia), fever (temperature > 38° C [100.4 F] (oral) / > 38.5° C [101.2 F] (tympanic) / > 39° C [102.2 F] (rectal)),
  • Minor signs and symptoms: headache, halitosis, dental pain, ear pressure/fullness, cough, fatigue,and radiological confirmation of diagnosis (presence of air/fluid level,total opacification,mucosal thickening > 10 mm)
  • 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

  • Recurrent sinusitis, sinusitis requiring other treatment than antibiotherapy, previous antibiotherapy in the last 30 days, previous corticotherapy, sinus surgery, sinus puncture / lavage in the last 7 days, known major obstructive anatomic / functional lesions in nasopharynx, symptomatic allergic sinusitis and / or rhinitis …

研究者

发起方
Aventis Intercontinental - Sanofi-aventis

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