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临床试验/JPRN-jRCT2080224658
JPRN-jRCT2080224658已完成3 期

ENT103 Phase 3 Clinical Study in Patients with Suppurative Otitis Media with Persistent or Prolonged Otorrhea

CEOLIA Pharma Co. Ltd0 个研究点目标入组 200 人开始时间: 2019年4月23日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
200

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

年龄范围
>= 15age old 至 ot applicable(—)
性别
All

入选标准

  • (1) Patients who are diagnosed with acute otitis media or perforated chronic otitis media caused by an infection.
  • (2) Patients who have clinically persistent suppurative otorrhea.
  • (3) Patients who obtained a written informed consent on the participation in this clinical study.

排除标准

  • (1) Patients who received antibiotic treatment for acute otitis media, exudative otitis media or perforated chronic otitis media within 3 months prior to enrollment.
  • (2) Patients who are diagnosed as eosinophilic otitis media, cholesteatoma otitis media, exudative otitis media or anti-neutrophil cytoplasmic antibody (ANCA) with associated vasculitis not to be treated by anti-microbial medication.
  • (3) Patients who have a trend on otitis media of fungal or tubercle bacillus infection (including infection to the tympanic membrane).
  • (4) Patients with otitis media with signs of viral infection (including infection to the tympanic membrane).
  • (5) Patients who have a mastoiditis.
  • (6) Patients who are observed to increase threshold of progressive pure sound bone conduction.
  • (7) Patients who are equipped with implantable otologic medical devices such as cochlear implants.
  • (8) Patients who have experienced inner ear dizziness within 3 months prior to enrollment.
  • (9) Patients who have infections that require systemic treatment with antibiotics.

研究者

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