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临床试验/CTRI/2021/03/032311
CTRI/2021/03/032311尚未招募未知

Risk of Progression In Incident Versus Prevalent Gonioscopic Angle Closure - IPAC

Massachusetts Eye and Ear Infirmary0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募

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

入选标准

  • Primary Angle Closure Suspect (PACS) >=180° degrees of occludable drainage angles without visible posterior trabecular meshwork [TM] Participants in the PACS group will need to meet criteria for PACS in both eyes
  • High Risk Open Angles (HROA) Individuals who have at least one eye open on gonioscopy (visible pigment TM>=270) who meet one of the following criteria
  • First-degree relatives of patients with Primary Angle Closure (PAC) / Primary Angle Closure Glaucoma (PACG)
  • Hyperopic by at least +2D and a corrected anterior chamber depth (cACD) <3 mm on optical biometry in at least one eye
  • Found to have narrow angles/shallow anterior chamber (defined as a van Herick grade <=2) and a cACD <3 mm on optical biometry in at least one eye

排除标准

  • Primary Angle Closure Suspect (PACS) participants will be excluded if they meet exclusion criteria in any eye. High Risk Open Angle (HROA) participants will be excluded if they meet exclusion criteria in the eye meeting HROA inclusion criteria.
  • Individuals <40 years of age
  • Individuals without capacity to consent/neuro cognitive disorders.
  • Presence of Peripheral Anterior Synechia (PAS), localized hyperpigmentation or other findings suggesting obstruction of Trabecular Meshwork (TM)
  • Intraocular Pressure (IOP) by Goldmann Applanation Tonometry >= 22 per Ocular Hypertension Treatment Study (OHTS) protocol12 (see methodology section). IOP will be measured at 2-month follow-up. The average of the baseline and 2-month follow-up IOP will be calculated. If the average is >=22, the participant will be excluded.
  • Evidence of glaucomatous optic neuropathy on examination according to the International Geographical and Epidemiological Ophthalmology (ISGEO) classification of glaucoma13:
  • Category 1 (structural and functional evidence): Vertical Cup Disc Ratio (VCDR) >=0.7, VCDR asymmetry >=0.2 or neuroretinal rim width <= 0.1 Cup Disc Ration (CDR) and definite Visual Field (VF) defect. No alternative explanation for CDR or VF findings.
  • Category 2 (advanced structural damaged with unproved field loss): VCDR >=0.85, VCDR asymmetry >=0.25 and incomplete VF. No alternative explanation for CDR findings.
  • Category 3 (Optic disc not seen. Field test impossible): IOP >=22 mm Hg and 3/60 visual acuity or visual acuity <3/60 and glaucoma surgery or documented history of glaucoma.
  • Visually significant cataract
  • Pseudophakia
  • Previous glaucoma laser or incisional surgery
  • Signs or symptoms of acute angle closure attack in any eye
  • Evidence of secondary glaucoma, other vision-threatening retinal pathology or systemic disease requiring frequent dilation, such as diabetic retinopathy and age-related macular degeneration.
  • Visual acuity <20/40

研究者

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