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临床试验/JPRN-jRCT1071230068
JPRN-jRCT1071230068招募中Unknown

Treatment protocols using azithromycin eye drops for recurrent cases bacterial blepharitis

ejima Ryohei0 个研究点目标入组 50 人开始时间: 2023年9月29日最近更新:
适应症

试验速览

阶段
Unknown
状态
招募中
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
>= 16age old 至 ot applicable(—)
性别
All

入选标准

  • 1) Patients 16 years of age or older with posterior blepharitis (with or without concurrent anterior blepharitis)
  • 2) Patients with a history of bacterial posterior blepharitis in the same eye previously treated with 1% azithromycin ophthalmic solution
  • 3) Patients with a total score of 4 or more of signs (eyelid redness eyelid margin redness, eyelash discharge, and conjunctival hyperemia) and symptoms (foreign body sensation, lacrimation) and a score of 1 or more of eyelid redness eyelid margin redness, and a score of 1 or more of symptoms.
  • 4) Patients who are able to administer ophthalmoplegia appropriately.
  • 5) Patients who understand the contents of the consent document and are able to give written consent
  • 6) Patients who are able to come to the hospital on the day of observation as instructed by the investigator.

排除标准

  • 1) Patients presenting with anterior blepharitis only
  • 2) Patients with eyelid diseases other than blepharitis (e.g., entropion, eyelid tumor)
  • 3) Patients with bacterial, fungal, viral, allergic, or other inflammatory diseases of the external eye (e.g., conjunctivitis, keratitis) other than blepharitis
  • 4) Patients with severe ocular surface disease
  • 5) Patients who have received topical or systemic administration of antibacterial agents (except 1% azithromycin ophthalmic solution), steroids, or immunosuppressive agents within the past 2 weeks
  • 6) Patients who have used 1% azithromycin ophthalmic solution within 3 weeks
  • 7) Patients deemed inappropriate for inclusion in this study by the principal investigator (investigator, etc.)
  • 8) Other patients who the principal investigator (investigator, etc.) determines to be inappropriate for the safe conduct of this study.

研究者

发起方
ejima Ryohei

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