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临床试验/NCT07606404
NCT07606404招募中不适用

Vitreoretinal Surgery for Full-Thickness Macular Hole: A Comparative Study of Ten Techniques

Kazakh Eye Research Institute1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2026年5月25日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
120
试验地点
1

研究概览

简要总结

This study compares ten modern vitreoretinal surgical techniques for full-thickness macular hole repair. Participants will be randomly assigned to one of the surgical approaches during pars plana vitrectomy, using stratified randomization based on macular hole size to ensure balanced groups. The main goal is to determine which technique provides the highest anatomical closure rate on optical coherence tomography (OCT) and the best visual outcomes. Follow-up visits are scheduled at Day 7, Month 1, and Year 1 after surgery to assess OCT findings, visual acuity, safety outcomes, and the need for reoperation.

详细描述

Full-thickness macular hole is a vision-threatening condition that is commonly treated with pars plana vitrectomy (PPV) and internal limiting membrane (ILM) peeling. While standard approaches achieve high closure rates in many cases, outcomes may vary depending on macular hole size and OCT morphology, and advanced surgical strategies (e.g., different ILM flap configurations, adjunctive biologic augmentation, hydrodissection, or grafting techniques) are increasingly used in clinical practice.

This single-center, randomized, parallel-group interventional study will compare ten PPV-based surgical techniques for full-thickness macular hole repair. Eligible participants will include adults with full-thickness macular hole across a broad range of minimum linear diameter (MLD), including MLD <250 µm. After eligibility confirmation and informed consent, participants will be randomized to one of the ten procedure groups. Randomization will be stratified by macular hole size into five predefined MLD strata to ensure balanced distribution of hole sizes across all intervention groups. Postoperative care and follow-up procedures will be standardized across groups according to the study protocol.

Follow-up visits are scheduled at Day 7, Month 1, and Year 1 after surgery and will include clinical examinations and OCT imaging. The primary endpoint is anatomical macular hole closure on OCT at the prespecified primary time point. Secondary endpoints include best-corrected visual acuity (BCVA), OCT-based morphologic recovery parameters, intraoperative and postoperative complication rates, reoperation rates, and adverse event information through Year 1. The study aims to generate evidence to guide selection of surgical technique based on macular hole morphometric and clinical characteristics while maintaining patient safety.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

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

入选标准

  • Adults aged ≥18 years.
  • Full-thickness macular hole (FTMH) eligible for pars plana vitrectomy (PPV).
  • Symptom duration ≤12 months.
  • Clear ocular media sufficient for high-quality OCT imaging.
  • No prior pars plana vitrectomy in the study eye.
  • No severe foveal atrophy on OCT.
  • Able and willing to comply with postoperative positioning and follow-up visits.
  • Written informed consent provided.

排除标准

  • A. Etiology-Related / Secondary Macular Holes:
  • Traumatic macular hole.
  • High myopia with posterior staphyloma (axial length >28 mm and/or spherical equivalent ≤-8.0 D).
  • Diabetic tractional retinal detachment (TRD) or significant tractional maculopathy.
  • Retinal vascular occlusion-related macular hole.
  • Uveitis-related macular hole.
  • Advanced age-related macular degeneration (AMD) with foveal atrophy.
  • B. Prior Interventions:
  • Any prior pars plana vitrectomy in the study eye.
  • C. Ocular Conditions That May Affect Outcomes or Safety:
  • Active or recent ocular infection or inflammation (e.g., uveitis, endophthalmitis, keratitis).
  • Uncontrolled glaucoma (intraocular pressure >28 mmHg despite treatment).
  • Media opacity precluding adequate OCT (e.g., dense cataract or corneal opacity).
  • Geographic atrophy involving the fovea.

研究者

发起方
Kazakh Eye Research Institute
申办方类型
Network
责任方
Principal Investigator
主要研究者

Kairat Ruslanuly

Senior Scientific Researcher

Kazakh Eye Research Institute

研究点 (1)

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