Purpose

The goal of this study is to determine whether using pilocarpine provides added benefit to the success of combined cataract + KDB surgery.

Condition

Eligibility

Eligible Ages
Between 30 Years and 100 Years
Eligible Genders
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Patients with ocular hypertension or open angle glaucoma undergoing combined cataract surgery with KDB

Exclusion Criteria

  • Patients with previous history of eye surgeries (including laser procedures)

Study Design

Phase
Phase 3
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Intervention Model Description
The "Treatment Group" will use 2% pilocarpine in the postoperative period in addition to standard postoperative drops (Prednisolone acetate and Ofloxacin). The "Control Group" will use only Prednisolone acetate and Ofloxacin, without pilocarpine.
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Pilocarpine, Prednisolone acetate and Ofloxacin
This group will use 2% pilocarpine in the postoperative period in addition to standard postoperative drops (Prednisolone acetate and Ofloxacin)
  • Drug: Pilocarpine
    pilocarpine hydrochloride ophthalmic solution 2% (20 mg/mL)
    Other names:
    • Isopto®
  • Drug: Prednisolone
    Prednisolone acetate ophthalmic suspension 1%
    Other names:
    • Pred Forte
  • Drug: Ofloxacin
    Ofloxacin Drops
    Other names:
    • Ocuflox
    • Floxin
Active Comparator
Prednisolone acetate and Ofloxacin (standard of care)
This group will use only Prednisolone acetate and Ofloxacin, without pilocarpine.
  • Drug: Prednisolone
    Prednisolone acetate ophthalmic suspension 1%
    Other names:
    • Pred Forte
  • Drug: Ofloxacin
    Ofloxacin Drops
    Other names:
    • Ocuflox
    • Floxin

Recruiting Locations

Montefiore Wakefield Campus
Bronx, New York 10466

Montefiore Medical Center
Bronx, New York 10467
Contact:
Wen-Jeng (Melissa) Yao, MD

More Details

Status
Recruiting
Sponsor
Montefiore Medical Center

Study Contact

Wen-Jeng (Melissa) Yao, MD
718-920-2020
WYAO@montefiore.org

Detailed Description

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[1]. 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[1]. 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[2]. Pilocarpine, a parasympathomimetic agent, is a glaucoma medication that works by causing contraction of the ciliary muscle leading to opening of the trabecular meshwork[3]. 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 rational 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.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.