ACTRN12621000688886尚未招募4 期
A double-blinded randomised control trial evaluating the efficacy of additional long-term low-dose Clarithromycin versus standard of care on post-operative symptomatic outcomes in the treatment of non-eosinophilic Chronic Rhinosinusitis in adults
Professor Alkis Psaltis0 个研究点目标入组 50 人开始时间: 2021年6月7日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 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
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Participants who meet ALL the following criteria will be offered inclusion in the study:
- •Those who have had symptoms of chronic rhinosinusitis that has been previously persistent for greater than 3 months
- •Are over 18 years of age
- •Are English speaking
- •Can give written informed consent
- •Have underwent endoscopic sinus surgery prior
- •Have a phenotype of non-eCRS on histological assessment
- •Disease control has not been established 6 weeks post-op
- •Can commit to return to the clinic for 12- and 18-weeks postoperative endoscopic examination.
排除标准
- •Participants who meet one the following criteria will be excluded from the study:
- •Allergy to macrolides
- •language other than English spoken
- •Pregnant or breastfeeding
- •History of cardiac disease
- •Allergy to steroids
- •Covid-19 positive
研究者
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