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Diagnostic Device
FDT visual field for Glaucoma
N/A
Waitlist Available
Led By Richard Lee, MD, PhD
Research Sponsored by University of Miami
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Adult patients (18 and over) who speak English, Spanish or Creole, and are capable of providing informed consent and who have a Humphrey Visual Field (HVF) test within the prior the 6 months preceding enrollment are eligible for enrollment in this non-invasive study. Patients will be recruited from among patients at the Bascom Palmer Eye Institute clinics during their regularly scheduled clinic visits. No advertising will be used to recruit patients.
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up the investigators anticipate to enroll the subjects over a period of 12 months. the estimated time required for data analysis is 6 months following enrollment of all subjects.
Awards & highlights
Study Summary
This trial will compare two types of eye exams to see which is more effective. 500 patients will be enrolled.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ the investigators anticipate to enroll the subjects over a period of 12 months. the estimated time required for data analysis is 6 months following enrollment of all subjects.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~the investigators anticipate to enroll the subjects over a period of 12 months. the estimated time required for data analysis is 6 months following enrollment of all subjects.
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Pattern of visual field loss in FDT visual fields as compared with standard HVF
Secondary outcome measures
Mean deviation (MD) in FDT visual fields as compared with standard HVF
Pattern standard deviation (PSD) in FDT visual fields as compared with standard HVF
Trial Design
1Treatment groups
Experimental Treatment
Group I: ExperimentalExperimental Treatment2 Interventions
FDT visual field will be compared to standard HVF in detecting glaucomatous visual field loss
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Who is running the clinical trial?
University of MiamiLead Sponsor
904 Previous Clinical Trials
409,730 Total Patients Enrolled
10 Trials studying Glaucoma
2,022 Patients Enrolled for Glaucoma
Richard Lee, MD, PhDPrincipal InvestigatorUniversity of Miami / Bascom Palmer Eye Institute
1 Previous Clinical Trials
40 Total Patients Enrolled
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