Pilocarpine Use After Kahook Goniotomy (PAACK)
Primary Purpose
Glaucoma
Status
Recruiting
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Pilocarpine
Prednisolone
Ofloxacin
Sponsored by
About this trial
This is an interventional treatment trial for Glaucoma focused on measuring Cataract, Glaucoma Surgery, Vision, Cataract Surgery, Eye surgery
Eligibility Criteria
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)
Sites / Locations
- Montefiore Wakefield CampusRecruiting
- Montefiore Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Pilocarpine, Prednisolone acetate and Ofloxacin
Prednisolone acetate and Ofloxacin (standard of care)
Arm Description
This group will use 2% pilocarpine in the postoperative period in addition to standard postoperative drops (Prednisolone acetate and Ofloxacin)
This group will use only Prednisolone acetate and Ofloxacin, without pilocarpine.
Outcomes
Primary Outcome Measures
Percentage of patients with lowering of intraocular pressure (IOP)
The percentage of patients who had a reduction in IOP of 20% or more from baseline
Secondary Outcome Measures
Proportion of patients whose regimen was reduced by 1 medication or more
Rate of progression towards further glaucoma surgeries
Full Information
NCT ID
NCT03933631
First Posted
April 26, 2019
Last Updated
July 13, 2023
Sponsor
Montefiore Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT03933631
Brief Title
Pilocarpine Use After Kahook Goniotomy
Acronym
PAACK
Official Title
A Prospective Randomized Control Trial of Pilocarpine Use After Combined Cataract/Kahook Dual Blade Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2019 (Actual)
Primary Completion Date
December 2025 (Anticipated)
Study Completion Date
December 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Montefiore Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
5. Study Description
Brief Summary
The goal of this study is to determine whether using pilocarpine provides added benefit to the success of combined cataract + KDB surgery.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glaucoma
Keywords
Cataract, Glaucoma Surgery, Vision, Cataract Surgery, Eye surgery
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
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.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
142 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Pilocarpine, Prednisolone acetate and Ofloxacin
Arm Type
Experimental
Arm Description
This group will use 2% pilocarpine in the postoperative period in addition to standard postoperative drops (Prednisolone acetate and Ofloxacin)
Arm Title
Prednisolone acetate and Ofloxacin (standard of care)
Arm Type
Active Comparator
Arm Description
This group will use only Prednisolone acetate and Ofloxacin, without pilocarpine.
Intervention Type
Drug
Intervention Name(s)
Pilocarpine
Other Intervention Name(s)
Isopto®
Intervention Description
pilocarpine hydrochloride ophthalmic solution 2% (20 mg/mL)
Intervention Type
Drug
Intervention Name(s)
Prednisolone
Other Intervention Name(s)
Pred Forte
Intervention Description
Prednisolone acetate ophthalmic suspension 1%
Intervention Type
Drug
Intervention Name(s)
Ofloxacin
Other Intervention Name(s)
Ocuflox, Floxin
Intervention Description
Ofloxacin Drops
Primary Outcome Measure Information:
Title
Percentage of patients with lowering of intraocular pressure (IOP)
Description
The percentage of patients who had a reduction in IOP of 20% or more from baseline
Time Frame
Up to 1 year
Secondary Outcome Measure Information:
Title
Proportion of patients whose regimen was reduced by 1 medication or more
Time Frame
Up to 1 year
Title
Rate of progression towards further glaucoma surgeries
Time Frame
Up to 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wen-Jeng (Melissa) Yao, MD
Phone
718-920-2020
Email
WYAO@montefiore.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wen-Jeng (Melissa) Yao, MD
Organizational Affiliation
Montefiore Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Montefiore Wakefield Campus
City
Bronx
State/Province
New York
ZIP/Postal Code
10466
Country
United States
Individual Site Status
Recruiting
Facility Name
Montefiore Medical Center
City
Bronx
State/Province
New York
ZIP/Postal Code
10467
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wen-Jeng (Melissa) Yao, MD
First Name & Middle Initial & Last Name & Degree
Wen-Jeng (Melissa) Yao, MD
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Pilocarpine Use After Kahook Goniotomy
We'll reach out to this number within 24 hrs