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临床试验/ACTRN12622001346763
ACTRN12622001346763尚未招募未知

Investigation of the effect of Intense Pulsed Light therapy on the signs and symptoms of contact lens discomfort.

niversity of New South Wales0 个研究点目标入组 48 人开始时间: 2022年10月19日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
入组人数
48

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

  • Age of 18 years and above
  • Willing to sign informed consent and comply with study schedule.
  • Normal vision defined as a minimum of 20/40 best corrected visual acuity in each eye.
  • Healthy ocular surface, defined as no fluorescein corneal staining of grade 2 or more after a single instillation of non-preserved fluorescein solution followed by examination 1 minute after installation, considering minimal staining of grade 1 as normal in contact lens wearers.
  • Normal external ocular examination with no eyelid deformation
  • Ability to cooperate with and undergo the required study procedures.
  • Contact lens wearers who have worn lenses for at least 6 months, used contact lenses for 3 weeks before the evaluation visit and used these lenses at least four times a week. Contact lenses should have been worn on a daily wear modality, where the lenses are worn for at least of 6 hours per day and remove the lenses before sleep.
  • Experience symptoms of contact lens discomfort (CLD), defined as CLDEQ-8 Questionnaire score more than 13.

排除标准

  • Any ocular or systemic disease that might influence the tear film
  • All forms of conjunctivitis, including allergic conjunctivitis
  • Any history of previous ocular surgery or trauma, including chalazion excision, oculoplastic
  • History of eyelid and periorbital skin disease or allergies in the past 1 month.
  • History of herpes zoster infection and any viral infection episode before.
  • Pregnancy, breast feeding
  • Skin cancer, user of photosensitive drugs /foods
  • Dark or deeply pigmented skin (Skin Fitzpatrick scale V/VI), which can be prone skin
  • damage, such as discoloration or scarring after IPL treatment.
  • Current use of any prescription on nonprescription ocular or systemic medications, including antihistamines.
  • Use of artificial tear preparations during the period 4 hours before all visits
  • Use of any ocular ointment during the 3 days before any study visit.
  • Have an history of epilepsy and migraine
  • Have any history of previous IPL treatment for dry eye.

研究者

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