Study Stopped
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Cataract Surgery on Advanced Age Related Macular Degeneration Patients
The Effects of Unilateral and Bilateral Cataract Extraction on Visual Function of Advanced Age-Related Macular Degeneration Patients.
1 other identifier
interventional
N/A
0 countries
N/A
Brief Summary
The degree at which cataract surgery improves visual function in patients with advanced age-related macular degeneration (Advanced AMD) has been an on-going topic of discussion. Our objective in this study is to determine if patients with Advanced AMD and concurrent cataracts will experience greater improvement in their quality of life from having cataract surgery on one or both eyes. The findings from this project will provide evidence for clinical decision making on whether performing bilateral cataract surgery on Advanced AMD patients is cost-effective and worth the second surgical intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Oct 2019
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 17, 2019
CompletedFirst Posted
Study publicly available on registry
August 5, 2019
CompletedStudy Start
First participant enrolled
October 1, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2019
CompletedOctober 4, 2021
September 1, 2021
2 months
July 17, 2019
September 27, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
Life style Questionnaire to determine change in visual function.
Our primary outcome will be a life style questionnaire (qualitative) to determine the change in visual function from baseline to after surgery. This questionnaire includes 25 close-ended questions that are graded on a 5 point grading scale from 1 (great difficulty due to vision) and 5 (no problem due to vision). The questions can also be graded as not applicable to an individuals life, or 0 being something there are no longer possible to do, due to vision. The 25 close-ended questions are divided into 4 sub-scales: 1. Distance Vision, Mobility, and Lighting (Q: 1-12) 2. Adjustment (Q:13-16) 3. Reading and Fine Work (Q: 17-21) 4. Activities of Daily Living (Q: 22-25) A total score can range from a 125 indicating best visual function to 0 indicating complete loss of visual function.
Through study completion, an average of 1 year
Secondary Outcomes (2)
Snellens Chart to determine change in visual acuity
Through study completion, an average of 1 year
Auto Refractive to determine change in visual acuity
Through study completion, an average of 1 year
Interventions
Patients with bilateral Advanced Age-related macular degeneration and concurrent cataracts will be receiving bilateral cataract surgery
Eligibility Criteria
You may qualify if:
- Patients above the age of fifty with both Advanced AMD and Cataracts bilaterally from the Okanagan Valley will be selected for this study.
- Patients who chose to have bilateral cataract surgery, were able to understand the research parameters, and had no other severe eye disease that may distort the studies results.
- Patients will be selected for the study according to the National Eye Institute definition of Advanced AMD.
- "Advanced AMD (AREDS category 4) is characterized by one or more of the following (in the absence of other causes) in one eye:
- Geographic atrophy of the RPE involving the foveal center.
- Neovascular maculopathy that includes the following:
- Choroidal neovascularization (CNV) defined as pathologic angiogenesis originating from the choroidal vasculature that extends through a defect in Bruch's membrane
- Serous and/or hemorrhagic detachment of the neurosensory retina or RPE
- Retinal hard exudates (a secondary phenomenon resulting from chronic intravascular leakage)
- Subretinal and sub-RPE fibrovascular proliferation
- Disciform scar (subretinal fibrosis)"
You may not qualify if:
- Severe intraoperative or postoperative complications such as retinal detachments, and capsule ruptures
- Inability to complete the required testing (auto-refractive and visual acuity)
- Inability to attend appointments
- Inability to complete the questionnaire with Co-I assistance
- Severe eye disease that may distort the studies results such as but not limited to Epithelial Basement Membrane Dystrophy (EBMD) and retinal detachments.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Clinical Assistant Professor
Study Record Dates
First Submitted
July 17, 2019
First Posted
August 5, 2019
Study Start
October 1, 2019
Primary Completion
December 1, 2019
Study Completion
December 1, 2019
Last Updated
October 4, 2021
Record last verified: 2021-09