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Glaucoma Management in the African-Derived Developing World Using Trabeculoplasty

Primary Purpose

Glaucoma

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Selective laser trabeculoplasty
Sponsored by
West Virginia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Glaucoma

Eligibility Criteria

30 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Afro-Caribbean ancestry
  • Ages 30 and above
  • Open-angle glaucoma (ISGEO criteria)
  • CDR≥0.7 or CDR asymmetry ≥0.2 or rim width ≤0.1 CDR with typical VF loss; or
  • CDR≥0.8 or CDR asymmetry ≥0.3 (if unable to get VF); or
  • VA <20/400 and IOP ≥ 32 mmHg (if unable to get VF or CDR)
  • Receiving ≤2 topical IOP-lowering medications
  • IOP between 17-35 mmHg in both eyes after 30-day washout

Exclusion Criteria:

  • Any glaucoma other than open-angle glaucoma
  • Advanced glaucoma (CDR > 0.9 or field loss in central 10º)
  • History of:
  • Prior glaucoma laser or surgery
  • Ocular inflammation within 3 months
  • Ocular trauma or intraocular surgery within 6 months

Sites / Locations

  • West Virginia University Eye Institute

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Treatment Cohort

Arm Description

All subjects will receive bilateral 360 degree Selective Laser Trabeculoplasty therapy in a single session, but will be randomized to one of three treatment sessions at times 0, Month 3 and Month 6. Subjects will be washed out of current IOP-lowering therapy 4-6 weeks pre-SLT. Subjects continuing on meds beyond time 0 will provide a comparator to early SLT to quantify regression to the mean.

Outcomes

Primary Outcome Measures

Probability of 12-month success (Proportion of subjects with 20% or greater IOP reduction 12 months following SLT)
Proportion of subjects with 20% or greater IOP reduction 12 months following SLT
Repeat probability of 12-month success (Proportion of subjects with 20% or greater IOP reduction from baseline 12 months after repeat SLT)
Generalizability of IOP-lowering efficacy to populations other than St. Lucia (significance of a site term in a predictive model of IOP reduction)
Evaluate significance of a site term in a predictive model of IOP reduction following SLT to determine if response to IOP is site dependent

Secondary Outcome Measures

Median survival time following initial SLT (Time from initial SLT to when 50% of subjects no longer manifest a 20% or greater reduction in IOP from baseline)
Time from initial SLT to when 50% of subjects no longer manifest a 20% or greater reduction in IOP from baseline
Mean IOP reduction (Descriptive analysis of mean (+/- SD) IOP reductions from baseline)
Descriptive analysis of mean (+/- SD) IOP reductions from baseline at each 12-month period following initial and repeat SLT, separately

Full Information

First Posted
January 26, 2015
Last Updated
June 17, 2021
Sponsor
West Virginia University
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1. Study Identification

Unique Protocol Identification Number
NCT02375009
Brief Title
Glaucoma Management in the African-Derived Developing World Using Trabeculoplasty
Official Title
Glaucoma Management in the African-Derived Developing World Using Trabeculoplasty
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Completed
Study Start Date
March 2015 (Actual)
Primary Completion Date
September 2018 (Actual)
Study Completion Date
September 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
West Virginia University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This proposal aims to evaluate selective laser trabeculoplasty (SLT) as a safe and effective therapy to control open-angle glaucoma and reduce the risk of progression to visual dysfunction or blindness in the African-derived developing world. If funded, this work will complete the characterization of SLT's safety and efficacy profile as a means of long-term disease control in this population. This work will support the translation of SLT into a structured public health initiative to reduce glaucoma-related vision loss throughout the African-derived developing world.
Detailed Description
Glaucoma is a leading cause of blindness in the African-derived developing world and represents a significant public health challenge as the disease burden is substantial. In Ghana, the prevalence of open-angle glaucoma over age 40 is 8.5%. In Barbados, the prevalence is 7.0%. In neighboring St. Lucia, the prevalence has been estimated at 8.8% with a 16% ten-year incidence of glaucoma-related blindness in one or both eyes. (In contrast, the prevalence in US adults is 1.9%.) The burden of glaucoma-related visual dysfunction is also substantial in the developing world. Because the application of medical and surgical therapies is limited by issues such as cost, availability, and limited regional surgical expertise, undertreatment is pervasive. Also, there is little access to low vision or vision rehabilitation services and minimal social support for the visually impaired. Laser trabeculoplasty may be a part of the solution to the developing world's burgeoning glaucoma burden. The treatment is fast, safe, minimally invasive and requires minimal post-treatment care; the equipment is portable; and the incremental cost of trabeculoplasty treatment is small once the equipment and expertise are on-site. Our recent study in St. Lucia demonstrated that laser trabeculoplasty lowers IOP by an amount likely to favorably alter the clinical course of glaucoma (versus no treatment) and has the potential to bend the glaucoma-related blindness curve in the African-derived developing world. Our long-term goal is to translate this finding through a public health initiative by establishing a pan-Caribbean glaucoma laser program to provide safe, effective, and cost-effective therapy for glaucoma in this underserved and overburdened region. Before this can happen, several important research questions remain unanswered regarding SLT in this population and comprise the specific aims of this proposal. What is the long-term efficacy of SLT in this population? Is repeat SLT effective once the IOP reduction of initial SLT wanes? Are the results obtained in St. Lucia generalizable to other developing nations populated by people of African descent? In this application, we propose a prospective cohort study in St. Lucia in which qualifying subjects with open-angle glaucoma will receive bilateral selective laser trabeculoplasty, will be followed to failure of initial SLT, and will undergo repeat SLT and again be followed to failure. The long-term safety and efficacy of both initial and repeat SLT in glaucoma patients of African descent will thus be established. Further, we will replicate the cohort study in Dominica to confirm external validity of the St. Lucia outcomes. This proposal is designed to answer the questions posed above and thus to complete the research phase of this project and facilitate translation of the research findings into the public health space. Considering the population of the African-derived developing world, the prevalence of glaucoma in this population, and the observed preliminary benefits of laser therapy, this project's output could ultimately reduce the risk of glaucoma-related visual dysfunction in hundreds of thousands of individuals throughout the developing world.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glaucoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
129 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment Cohort
Arm Type
Experimental
Arm Description
All subjects will receive bilateral 360 degree Selective Laser Trabeculoplasty therapy in a single session, but will be randomized to one of three treatment sessions at times 0, Month 3 and Month 6. Subjects will be washed out of current IOP-lowering therapy 4-6 weeks pre-SLT. Subjects continuing on meds beyond time 0 will provide a comparator to early SLT to quantify regression to the mean.
Intervention Type
Procedure
Intervention Name(s)
Selective laser trabeculoplasty
Intervention Description
laser therapy to trabecular outflow pathway of the eye to lower intraocular pressure, delivered to 360 degrees of both eyes in a single session
Primary Outcome Measure Information:
Title
Probability of 12-month success (Proportion of subjects with 20% or greater IOP reduction 12 months following SLT)
Description
Proportion of subjects with 20% or greater IOP reduction 12 months following SLT
Time Frame
12 months
Title
Repeat probability of 12-month success (Proportion of subjects with 20% or greater IOP reduction from baseline 12 months after repeat SLT)
Time Frame
12 months after as-needed repeat SLT
Title
Generalizability of IOP-lowering efficacy to populations other than St. Lucia (significance of a site term in a predictive model of IOP reduction)
Description
Evaluate significance of a site term in a predictive model of IOP reduction following SLT to determine if response to IOP is site dependent
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Median survival time following initial SLT (Time from initial SLT to when 50% of subjects no longer manifest a 20% or greater reduction in IOP from baseline)
Description
Time from initial SLT to when 50% of subjects no longer manifest a 20% or greater reduction in IOP from baseline
Time Frame
Through up to five years of follow-up
Title
Mean IOP reduction (Descriptive analysis of mean (+/- SD) IOP reductions from baseline)
Description
Descriptive analysis of mean (+/- SD) IOP reductions from baseline at each 12-month period following initial and repeat SLT, separately
Time Frame
through up to five years of follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Afro-Caribbean ancestry Ages 30 and above Open-angle glaucoma (ISGEO criteria) CDR≥0.7 or CDR asymmetry ≥0.2 or rim width ≤0.1 CDR with typical VF loss; or CDR≥0.8 or CDR asymmetry ≥0.3 (if unable to get VF); or VA <20/400 and IOP ≥ 32 mmHg (if unable to get VF or CDR) Receiving ≤2 topical IOP-lowering medications IOP between 17-35 mmHg in both eyes after 30-day washout Exclusion Criteria: Any glaucoma other than open-angle glaucoma Advanced glaucoma (CDR > 0.9 or field loss in central 10º) History of: Prior glaucoma laser or surgery Ocular inflammation within 3 months Ocular trauma or intraocular surgery within 6 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tony Realini, MD, MPH
Organizational Affiliation
West Virginia University Eye Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
West Virginia University Eye Institute
City
Morgantown
State/Province
West Virginia
ZIP/Postal Code
26505
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
33836987
Citation
Realini T, Shillingford-Ricketts H, Burt D, Balasubramani GK. Clinical outcomes following selective laser trabeculoplasty in Afro-Caribbean patients with glaucoma at high risk for progression. Br J Ophthalmol. 2022 Sep;106(9):1235-1239. doi: 10.1136/bjophthalmol-2020-317117. Epub 2021 Apr 9.
Results Reference
derived
PubMed Identifier
29965865
Citation
Realini T, Shillingford-Ricketts H, Burt D, Balasubramani GK. West Indies Glaucoma Laser Study (WIGLS)-2: Predictors of Selective Laser Trabeculoplasty Efficacy in Afro-Caribbeans With Glaucoma. J Glaucoma. 2018 Oct;27(10):845-848. doi: 10.1097/IJG.0000000000001018.
Results Reference
derived

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Glaucoma Management in the African-Derived Developing World Using Trabeculoplasty

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