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
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