跳至主要内容
临床试验/CTIS2023-504451-27-00
CTIS2023-504451-27-00进行中(未招募)1 期

Treating socket discharge and discomfort: randomized test of vitamin A ointment, low-dose steroids and artificial tears

Amsterdam UMC0 个研究点目标入组 100 人开始时间: 2023年3月13日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
100

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
18 至 65+(—)
性别
All

入选标准

  • Patients wearing an ocular prosthesis and Excess mucopurulent discharge and/or discomfort

排除标准

  • - Subjects < 16 years old - Subjects expected to be incapable to understand the study or fill-out the questionnaires. - Patients with treatable acquired medical issues of the socket (ie new conjunctival cyst, exposed implant). If the patients still have mucopurulent discharge and discomfort after removal/treatment of the irritative factor, they can be included. - Patients with transient complaints from suspected (sub) acute infections for which antibiotics are prescribed. If the patients still have mucopurulent discharge and discomfort after treatment, they can be included. - Patients with scratched, or irregular prostheses, or with latest polishing more than one year ago, should first have their prosthesis polished or renewed. If the patients still have mucopurulent discharge and discomfort after these improvements than they can be included. - The model of the prosthesis should first be adapted if a wrong fit is suspected (ie large empty space, pressure points). If the patients still have mucopurulent discharge and discomfort after these improvements than they can be included.

研究者

发起方
Amsterdam UMC

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