A Prospective Randomized Control Trial of Pilocarpine Use After Combined Cataract/Kahook Dual Blade Surgery
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 142
- 试验地点
- 2
- 主要终点
- Percentage of patients with lowering of intraocular pressure (IOP)
研究概览
简要总结
The goal of this study is to determine whether using pilocarpine provides added benefit to the success of combined cataract + Kahook Dual Blade (KDB) surgery.
详细描述
Glaucoma is the leading cause of irreversible blindness worldwide, and its treatment consists of lowering intraocular pressure to prevent damage to the optic nerve and loss of vision. Current methods for lowering intraocular pressure (IOP) include topical and oral medications, laser trabeculoplasty, microincisional glaucoma surgery (MIGS), and traditional incisional surgeries such as trabeculectomy and aqueous tube shunts. MIGS have become more popular in recent years as less invasive methods than traditional surgeries that effectively reduce IOP and help reduce the medication burden on patients. There are multiple available MIGS procedures, most of which act by increasing trabecular outflow. One such procedure is the goniotomy via Kahook Dual Blade (KDB), which is usually performed in combination with cataract surgery. KDB is an FDA approved device used to perform a goniotomy via an internal approach. Strips of the nasal angle trabecular meshwork are removed providing a direct pathway for aqueous outflow from the anterior chamber into the collector channels.
Pilocarpine, a parasympathomimetic agent, is a glaucoma medication that works by causing contraction of the ciliary muscle leading to opening of the trabecular meshwork. Due to its frequent dosing requirement and large number of ocular and systemic side effects, pilocarpine has largely fallen out of favor for the treatment of primary open angle glaucoma (POAG), except in patients for whom few other alternatives exist. However, pilocarpine is often used after goniotomy surgery. The rationale for its use after goniotomy procedure is for its miotic effect, which theoretically may prevent the formation of peripheral anterior synechiae. Formation of peripheral anterior synechiae can lead to the closure of the cleft that is generated and the possibility of failure of the procedure. While the theoretical benefit of pilocarpine has been proposed, its actual benefit has never been proven. This study will evaluate whether goniotomy via KDB / Cataract surgery without pilocarpine is non-inferior to the same surgery procedure followed by treatment with pilocarpine.
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
- None
入排标准
- 年龄范围
- 30 Years 至 100 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with ocular hypertension or open angle glaucoma undergoing combined cataract surgery with KDB in a single surgical center at Montefiore Medical Center with a single provider
排除标准
- •Patients with previous history of eye surgeries (including laser procedures)
研究组 & 干预措施
Pilocarpine, Prednisolone acetate and Ofloxacin
This group will use 2% pilocarpine in the postoperative period, for one month, in addition to standard postoperative drops (Prednisolone acetate and Ofloxacin)
干预措施: Pilocarpine (Drug)
Pilocarpine, Prednisolone acetate and Ofloxacin
This group will use 2% pilocarpine in the postoperative period, for one month, in addition to standard postoperative drops (Prednisolone acetate and Ofloxacin)
干预措施: Prednisolone (Drug)
Pilocarpine, Prednisolone acetate and Ofloxacin
This group will use 2% pilocarpine in the postoperative period, for one month, in addition to standard postoperative drops (Prednisolone acetate and Ofloxacin)
干预措施: Ofloxacin (Drug)
Prednisolone acetate and Ofloxacin (standard of care)
This group will use only the standard Prednisolone acetate and Ofloxacin, without pilocarpine.
干预措施: Prednisolone (Drug)
Prednisolone acetate and Ofloxacin (standard of care)
This group will use only the standard Prednisolone acetate and Ofloxacin, without pilocarpine.
干预措施: Ofloxacin (Drug)
结局指标
主要结局
Percentage of patients with lowering of intraocular pressure (IOP)
时间窗: From baseline to 1 year following procedure
The percentage of patients who had a reduction in IOP of 20% or more from baseline will be summarized by study arm using descriptive statistics.
次要结局
- Proportion of patients whose regimen was reduced by 1 medication or more(Up to 1 year following procedure)
- Hypotensive medications(Up to 1 year following procedure)
- Rate of progression towards further glaucoma surgery - Humphrey Visual Fields (HVF)(Up to 1 year following procedure)
- Rate of progression towards further glaucoma surgery - Optical Coherence Tomography (OCT)(Up to 1 year following procedure)
- Need for additional glaucoma surgery(Up to 1 year following procedure)
