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临床试验/NCT07774637
NCT07774637招募中不适用

Structural and Functional Determinants of Surgical Outcomes in Vitrectomy for Myopic Foveoschisis

Singapore National Eye Centre1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年6月10日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
1
主要终点
visual acuity

研究概览

简要总结

This prospective pilot study evaluates factors that predict outcomes after vitrectomy for myopic foveoschisis (MFS), a sight-threatening complication of high myopia that can lead to progressive visual loss, foveal detachment, macular holes, and retinal detachment. Although vitrectomy can relieve traction and improve retinal anatomy, the optimal timing of surgery and the factors associated with visual recovery remain uncertain, particularly in patients with relatively good pre-operative vision.

The study will recruit 30 adults aged 40-90 years from Singapore National Eye Centre surgical retina clinics. Participants must have high myopia (worse than -6 dioptres and axial length >26 mm) with MFS requiring surgery because of progressive vision loss with OCT-confirmed deterioration over six months and/or foveal detachment. Patients with other ocular diseases or conditions that could confound imaging or functional testing, poor surgical candidacy, cognitive impairment, or ungradable imaging will be excluded.

Participants will undergo standard-of-care 23- or 25-gauge pars plana vitrectomy, with fovea-sparing internal limiting membrane peeling or flap, possible gas tamponade, and cataract surgery where clinically indicated. The research does not alter the usual surgical approach; its main purpose is to collect structural and functional outcome data over 12 months.

Assessments will be performed at baseline and during postoperative follow-up, including best-corrected visual acuity, refracted logMAR visual acuity, microperimetry, M-chart testing for metamorphopsia, contrast sensitivity using the Manifold Contrast Vision Meter, and swept-source OCT. OCT measures will include central retinal thickness, foveal detachment, inner and outer macular schisis, lamellar holes, and epiretinal membrane. Demographic and clinical variables, including age, sex, co-morbidities, and lens status, will also be collected.

The primary functional outcome is stable or improved best-corrected visual acuity. Anatomical success is defined as improvement in retinoschisis and resolution of pre-existing foveal detachment. The investigators hypothesise that improvement can occur across a range of MFS severities, and that baseline OCT features and functional measures can help predict 12-month surgical success.

As a pilot study, no formal sample-size calculation is planned. Analyses will describe clinical characteristics, compare outcomes between better and poorer pre-operative visual-acuity groups, and use multivariable logistic regression to identify prognostic factors. Risks are limited to usual surgical complications and confidentiality risks; all study tests are non-invasive. Data will be securely stored, access restricted to the study team, and participants will provide informed consent.

Parallel studies will be conducted with overseas collaborators.

详细描述

  • Detailed Study Summary

  • Study title:** *Structural and functional determinants of surgical outcomes in vitrectomy for myopic foveoschisis*

  • Protocol number:** R2028/71/2023 (SHF-SNEC 0923-2)

  • Version/date:** Version 1.0, 20 September 2023

  • Study site:** Singapore National Eye Centre (SNEC)

  • Principal investigator:** Tsai Shih Hsiang Andrew

  • Funding:** SHF SNEC grant

  • Background and rationale

Myopic foveoschisis (MFS) is a potentially sight-threatening macular complication in highly myopic eyes, particularly those with posterior staphyloma. It is characterised by splitting of retinal layers at the macula and may progress to foveal detachment, full-thickness macular hole, macular-hole retinal detachment, macular atrophy, and substantial visual impairment. MFS has been reported in approximately 8-34% of patients with posterior staphyloma. Optical coherence tomography (OCT) has become central to diagnosis and monitoring because it allows detailed assessment of the degree of macular schisis and identifies complications that may require surgery.

The accepted surgical treatment for MFS requiring intervention is pars plana vitrectomy, with techniques directed at relieving anteroposterior and tangential vitreomacular traction. These techniques may include internal limiting membrane (ILM) peeling or fovea-sparing ILM flap procedures, sometimes with gas tamponade. The intended result is restoration of retinal anatomy and improvement or preservation of visual function.

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
40 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • The target population is 30 adults with high myopia and MFS requiring vitrectomy.
  • inclusion critieria
  • Be 40-90 years old.
  • Have high myopia, defined as refractive error worse than -6 dioptres and axial length longer than 26 mm.
  • Be mentally competent to provide informed consent.
  • Have MFS that meets clinical criteria for surgical intervention, specifically:progressively worsening vision that correlates with structural OCT deterioration over six months; and/or foveal detachment.

排除标准

  • patients with ocular disorders, prior treatments, or other conditions that could affect structural imaging or functional measurements
  • corneal opacity
  • dense cataract
  • vitreous haemorrhage
  • central serous chorioretinopathy
  • prior retinal laser photocoagulation or photodynamic therapy
  • previous or concurrent retinal detachment
  • retinal dystrophies
  • macular scarring
  • retinal vascular occlusion
  • ocular ischaemic syndrome
  • ungradable OCT/OCTA imaging.
  • Patients who are cognitively impaired or prisoners are excluded.
  • Patients considered poor highly myopic surgical candidates are also excluded, including those with myopic choroidal neovascularisation, macular scar, or complete macular atrophy according to the ATN classification.
  • Participants may also be discontinued from study assessments if OCT imaging is unsatisfactory or ungradable, or if they are unable to complete functional tests such as microperimetry, contrast sensitivity testing, or M-chart assessment.

结局指标

主要结局

visual acuity

时间窗: 12 months

change in best corrected snellen chart visual acuity

anatomical success

时间窗: 12 months

change in retinoschisis and resolution of pre-existing foveal detachment as measured via optical coherence tomography in microns

次要结局

未报告次要终点

研究者

申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Andrew Tsai

Clinical Associate Professor

Singapore National Eye Centre

研究点 (1)

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