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临床试验/NCT02995746
NCT02995746终止不适用

Intravitreal Dexamethasone Implant for Persistent Macular Thickening and Edema After Vitrectomy for Epiretinal Membrane: A Pilot Study

Wills Eye1 个研究点 分布在 1 个国家目标入组 3 人开始时间: 2016年1月28日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
发起方
入组人数
3
试验地点
1
主要终点
Mean central macular thickness (CMT) on SD-OCT at 1 month, 3 months, and 6 months after intravitreal injection of dexamethasone implant

研究概览

简要总结

This study seeks to evaluate the effect of the intravitreal 0.7mg dexamethasone implant on central macular thickness and visual acuity in those patients with persistent macular edema after pars plana vitrectomy for epiretinal membrane.

详细描述

Macular edema is a relatively common occurrence after pars plana vitrectomy. Kim et al described that 47% of eyes undergoing vitrectomy for epiretinal membrane, macular hole, or vitreous hemorrhage had evidence of macular thickening on optical coherence tomography scan.1 Post-vitrectomy macular edema can limit potential visual acuity gain from removal of a symptomatic epiretinal membrane. Typical treatment of post-operative macular edema consists of topical non-steroidal anti-inflammatory drugs (NSAIDs) and topical corticosteroids; however, there are still resistant cases with refractory macular thickening.

The dexamethasone intravitreal implant (Ozurdex; Allergan, Irvine, CA) is currently FDA-approved for the treatment of posterior uveitis as well as macular edema secondary to retinal vein occlusion and diabetic retinopathy. Furino et al reported a retrospective series describing how a single injection of the 0.7mg dexamethasone intravitreal implant resulted in a substantial increase in best-corrected visual acuity (BCVA) and a decrease in central macular thickness (CMT) on spectral-domain optical coherence tomography (SD-OCT) in 8 patients with persistent macular thickening after pars plana vitrectomy for epiretinal membrane. There has been no prospective study evaluating the efficacy of this pharmacologic agent in this setting.

As such, the purpose of this study is to prospectively evaluate the effect of the intravitreal 0.7mg dexamethasone implant on CMT and BCVA in those patients with persistent macular edema after pars plana vitrectomy for epiretinal membrane.

The results of this study will help delineate whether the intravitreal dexamethasone implant has efficacy in improving CMT and/or visual acuity in those patients with refractory macular thickening after pars plana vitrectomy for epiretinal membrane.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient of the Wills Eye Institute Retina service, including all Mid-Atlantic Retina offices
  • Volunteer patients age 18 years and older
  • Healthy enough to participate in the study
  • Willing and able to consent to participation in the study
  • History of pars plan vitrectomy for symptomatic epiretinal membrane at least 3 months prior to study enrollment date
  • BCVA of 20/40 or worse
  • CMT of at least 400 micrometers with or without cystoid macular edema on SD-OCT
  • Prior treatment with topical NSAIDs without resolution of macular thickening or visual acuity improvement

排除标准

  • Advanced glaucoma (cup-disc ratio of 0.8 or greater)
  • History of glaucoma filtering or tube shunt implant surgery
  • Steroid responsive intraocular hypertension
  • Diabetic retinopathy
  • History of uveitis
  • Use of systemic or intraocular corticosteroids
  • Active or suspected ocular or periocular infections
  • Other confounding intraocular pathology

研究组 & 干预措施

0.7mg dexamethasone intravitreal implant

Experimental

Single intravitreal implantation of 0.7mg dexamethasone with a six month follow up period

干预措施: Dexamethasone (Drug)

结局指标

主要结局

Mean central macular thickness (CMT) on SD-OCT at 1 month, 3 months, and 6 months after intravitreal injection of dexamethasone implant

时间窗: Change in mean macular thickness baseline at 6 months

次要结局

  • Visual acuity(Change in visual acuity baseline at 6 months)

研究者

发起方
Wills Eye
申办方类型
Other
责任方
Principal Investigator
主要研究者

Allen C. Ho, MD

MD

Wills Eye

研究点 (1)

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