Detection of Topographic Residual Acuity in Patients With Age Related Macular Degeneration
1 other identifier
interventional
30
1 country
1
Brief Summary
Standard perimetry provides information on topographical retinal sensitivity to light stimuli, however the said locus is not necessarily the preferred locus for fixation. Standard perimetry could also be used as a way for macular scotoma mapping, indirectly showing the fixation locus. Topographic acuity at the preferred retinal locus can be determined if correlation between loci with high sensitivity, eccentric fixation loci and potential visual acuity measurements are correlated. PURPOSE OF THE STUDY: Determination of visual acuity at preferred retinal locus in Low Vision patients with ARMD using eye standard automated and computerized perimetry methods.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Apr 2006
1 active site
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
Study Start
First participant enrolled
April 1, 2006
CompletedFirst Submitted
Initial submission to the registry
May 23, 2006
CompletedFirst Posted
Study publicly available on registry
May 24, 2006
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2008
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2008
CompletedMay 28, 2008
November 1, 2006
1.8 years
May 23, 2006
May 22, 2008
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Location of eccentric retinal locus of highest fixation accuracy
Secondary Outcomes (1)
Location of eccentric locus with best retinal sensitivity
Interventions
Eligibility Criteria
You may qualify if:
- AMD with documented pathology
- Low Vision both eyes
- BCVA 20/50-20/400 in best eye
You may not qualify if:
- Cognitive impairment
- Other retinal pathology
- Previous retinal surgery
- Significant media opacity
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Dr S N Markowitz
Toronto, Ontario, M6H 2H1, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Samuel Markowitz, MD
University Health Network, Toronto
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
May 23, 2006
First Posted
May 24, 2006
Study Start
April 1, 2006
Primary Completion
January 1, 2008
Study Completion
January 1, 2008
Last Updated
May 28, 2008
Record last verified: 2006-11