跳至主要内容
临床试验/NCT05906212
NCT05906212进行中(未招募)不适用

Use of Anterior Lens Capsule as a Spacer in the Deep Sclerectomy _ Phacoemulsification: A Randomized Clinical Trial

Shahid Beheshti University of Medical Sciences1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2023年5月16日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
66
试验地点
1
主要终点
Change from baseline intraocular pressure at month 3 follow up

研究概览

简要总结

In this randomized clinical trial, patients with concomitant glaucoma and cataract candidate for non-penetrating deep sclerectomy (NPDS) and phacoemulsification (PE) and subtenon mitomycin injection will be enrolled. Patients will randomly be allocated to two groups ["NPDS and PE and autotransplantation of human anterior lens capsule (ALC)" and "NPDS and PE" alone]. Exclusion criteria will be the patients with prior ocular surgery, neovascular glaucoma, uveitis, or compromised ocular surface. The intervention group will be undergoing NPDS and PE with the use of an ALC as the spacer in the intrascleral lake. The control group will be undergoing NPDS and PE without any spacer. The primary outcome will be intraocular pressure measured on days 1, 3, 7, months 1, 3, 6, and 12. The secondary outcomes will be surgical success rate (complete and qualified), the number of glaucoma medications, best-corrected visual acuity, surgical complications, and the need for needling and laser goniopuncture measured at the same intervals. The complete success rate will be defined as intraocular pressure less than 18 mmHg with a 20 percent reduction without anti-glaucoma medication. The qualified success rate will be defined as intraocular pressure less than 18 mmHg with a 20 percent reduction with anti-glaucoma medication.

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, Investigator)

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

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Change from baseline intraocular pressure at month 3 follow up

时间窗: Baselines and month 3 follow up

The intraocular pressure will be assessed by Goldmann Applanation Tonometry at baselines and month 3 follow up

Change from baseline intraocular pressure at month 12 follow up

时间窗: Baselines and month 12 follow up

The intraocular pressure will be assessed by Goldmann Applanation Tonometry at baselines and month 12 follow up

Change from baseline intraocular pressure at month 1 follow up

时间窗: Baselines and month 1 follow up

The intraocular pressure will be assessed by Goldmann Applanation Tonometry at baselines and month 1 follow up

Change from baseline intraocular pressure at month 6 follow up

时间窗: Baselines and month 6 follow up

The intraocular pressure will be assessed by Goldmann Applanation Tonometry at baselines and month 6 follow up

次要结局

  • Need to postoperative needling and laser goniopuncture at month 1 follow up(Month 1 follow up)
  • The complete success rate at month 12 follow up(Month 12 follow up)
  • The qualified success rate at the month 12 follow up(Month 12 follow up)
  • The qualified success rate at the month 1 follow up(Month 1 follow up)
  • The complete success rate at month 1 follow up(Month 1 follow up)
  • The qualified success rate at month 3 follow up(Month 3 follow up)
  • Change from baseline the number of glaucoma medications at month 6 follow up(Baseline and month 6 follow up)
  • The complete success rate at month 3 follow up(Month 3 follow up)
  • The complete success rate at month 6 follow up(Month 6 follow up)
  • The qualified success rate at month 6 follow up(Month 6 follow up)
  • Change from baseline the number of glaucoma medications at month 12 follow up(Baseline and month 12 follow up)
  • Complications at month 6 follow up(Month 6 follow up)
  • Need to postoperative needling and laser goniopuncture at month 3 follow up(Month 3 follow up)
  • Complications at month 3 follow up(Month 3 follow up)
  • Change from baseline the number of glaucoma medications at month 1 follow up(Baseline and month 1 follow up)
  • Need to postoperative needling and laser goniopuncture at month 6 follow up(Month 6 follow up)
  • Need to postoperative needling and laser goniopuncture at month 12 follow up(Month 12 follow up)
  • Change from baseline the number of glaucoma medications at month 3 follow up(Baseline and month 3 follow up)
  • Change from baseline the best-corrected visual acuity at month 6 follow up(Baseline and month 6 follow up)
  • Change from baseline the best-corrected visual acuity at month 12 follow up(Baseline and month 12 follow up)
  • Complications at month 1 follow up(Month 1 follow up)
  • Complications at month 12 follow up(Month 12 follow up)

研究者

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

Mohammadali Javadi, MD

Head of Ophthalmic Research Center

Shahid Beheshti University of Medical Sciences

研究点 (1)

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