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临床试验/NCT03292796
NCT03292796已完成2 期

A Randomised Control Study to Investigate if the Continuation of Prostaglandin Analogue Treatments in the Post-operative Phase of Glaucoma Patients Undergoing Cataract Surgery Increases the Incidence of Cystoid Macular Oedema.

Julie Dawson1 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2016年12月7日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
发起方
Julie Dawson
入组人数
56
试验地点
1
主要终点
Occurrence of cystoid macula oedema (CMO) at 4 weeks post operatively

研究概览

简要总结

Post-operative cystoid macular oedema (CMO) is a common complication causing visual loss following routine cataract surgery. This complication is more prevalent in eyes with excessive inflammation as they heal from surgery.

Prostaglandin analogues (PGA) are the commonest first line drugs used in the long-term treatment of primary open angle glaucoma (POAG)- where they reduce the pathologically high pressure in the eye. Prostaglandins are inflammatory mediators.

In the post-operative care of glaucoma patients undergoing cataract surgery, there is a clinical dilemma whether to stop or continue the use of prostaglandin eye drops. Clinical practice is completely dichotomized between continuing and stopping PGA treatment in the postoperative period. There is conflicting scientific literature on the effect of PGA on the incidence of CMO; and only a single randomized control trial (Miyake K, Arch Ophthalmol 1999, 117:34-40), where the post operative regime is not applicable to present practice, compared the incidence of CMO following routine cataract surgery in POAG on PGA.

详细描述

This study aims to answer the common clinical question of whether or not to stop PGA after routine cataract surgery. Cataract surgery is the commonest operation performed on the NHS and the prevalence of glaucoma is 5% in the population over 80 years old. Thus the clinical dilemma is a common one.

A current literature search reveals that a divided opinion over whether PGAs do increase the incidence of CMO. No study has yet established a causal relationship between the use of PGAs and the development of CMO. Anecdotal reports and small case series have associated peri-operative PGA use with the occurrence of CMO (Henderson BA et al, 2007 J Cataract Refract Surg 33:1550-1558; Moroi SE et al, 1999, Ophthalmology 106:1024-1029). Whilst, in direct contrast, other authors argue CMO as a rare phenomenon and the causative relationship is debated (Schumer RA et al 2000, Curr Opin Ophthalmol 11:94-100; Miyake K et al 2003 J Cataract Refract Surg 29:1800-1810)

The most similar previous study to the one proposed, was by Miyake K et al. (Arch Ophthalmol 1999, 117:34-40). The key difference, though, is in the postoperative drop regime of fluorometholone and diclofenac in that paper and current UK clinical practice of using dexamethasone. In terms of study design, this paper used an invasive method of investigating CMO by fundus fluorescein angiography compared to OCT proposed here.

A recent case report by Agange N & Mosaed S (Journal of Ophthalmology, 2010) concludes with 'conclusions about causal relationships cannot be made without well-designed, prospective clinical trials addressing this issue'.

This study will therefore use drops that are routinely used in current UK clinical practice and add to the body of evidence that helps answer the question should PGAs be continued after cataract surgery so as to prevent the progression of glaucoma in patients.

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
Single (Outcomes Assessor)

盲法说明

  • The patient is not masked as to treatment group and are aware of whether they are to continue or stop the PGA drops

  • The care providers are not masked as to treatment group

  • Outcome assessors are masked as to the patient's treatment group for their analysis of the OCT scans over the 4 week peri-operative period.

  • The scans are recorded with only the randomised identifier.

  • This is to reduce bias in the analysis of the scans

  • Unmasking of each patient will occur after their analysis of their week 4 OCT scan

入排标准

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

入选标准

  • Primary open-angle glaucoma and ocular hypertensive subjects undergoing cataract surgery (routine phacoemulsification and intraocular lens implantation) AND on current topical glaucoma treatment with a prostaglandin analogue eye drop for at least 2 months prior to cataract surgery.
  • Subjects capable of giving informed consent

排除标准

  • Subjects with additional risk factors for macula oedema (eg. diabetic retinopathy, previous macula oedema, uveitis)
  • Subjects with advanced glaucoma
  • Advanced visual field loss (Humphrey Mean Deviation >-12dB)
  • Advanced glaucomatous disc changes (vertical cup-to-disc ratio >0.9)
  • Subjects with non-controlled intraocular pressure (IOP) (pre-operative IOP >22 mmHg)
  • Any contra-indication to the use of topical prostaglandin drops
  • Any contra-indication to the use of routine post-operative dexamethasone 0.1% eye drops
  • Pregnancy
  • Patients unable to give informed consent
  • Intra-operative complication during cataract phacoemulsification and intraocular lens implantation

研究组 & 干预措施

Stop prostaglandin eye drops post op

Other

Stop prostaglandin eye drops post operatively. Prostaglandins either stopped or continued after cataract surgery. Latanoprost Travaprost Bimatoprost Tafluprost

干预措施: Prostaglandins (Drug)

Continue prostaglandin eye drops post op

Other

Continue prostaglandin eye drops post operatively Prostaglandins either stopped or continued after cataract surgery. Latanoprost Travaprost Bimatoprost Tafluprost

干预措施: Prostaglandins (Drug)

结局指标

主要结局

Occurrence of cystoid macula oedema (CMO) at 4 weeks post operatively

时间窗: 4 weeks post operatively

Occurrence of cystoid macula oedema (CMO) at 4 weeks post operatively.Cystoid macular oedema will be defined as an increase in the central macula thickness on the OCT with characteristic intraretinal changes in the 4 weeks following surgery.

次要结局

  • Intraocular pressure (IOP) at 4 weeks post-operatively.(4 weeks post operatively)

研究者

发起方
Julie Dawson
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Julie Dawson

Research Services Manager

Norfolk and Norwich University Hospitals NHS Foundation Trust

研究点 (1)

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