Tracking Optical Coherence Tomography
2 other identifiers
observational
100
1 country
1
Brief Summary
The purpose of this research study is to evaluate an investigational system that may allow doctors to show images of the different parts inside the eye that show greater detail than current equipment can produce.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Oct 2004
Longer than P75 for all trials
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
October 1, 2004
CompletedFirst Submitted
Initial submission to the registry
June 19, 2006
CompletedFirst Posted
Study publicly available on registry
June 23, 2006
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2011
CompletedOctober 25, 2016
July 1, 2011
6.2 years
June 19, 2006
October 24, 2016
Conditions
Keywords
Eligibility Criteria
Subject can range between 18 to 85 years old. They can be healthy or diseased. Recruiting males and females.
You may qualify if:
- Healthy individuals (this includes women of child-bearing potential) who are familiar with vision experiments and ophthalmic equipment, all over 18 years.
- Subjects will have a retinal screening if they are over 50 years old or have a known risk factor for eye disease, such as family history of age related macular degeneration or cardiovascular disease.
- Patients with retinal and choroidal disease: age related maculopathy or age related macular degeneration, diabetic retinopathy, glaucoma.
You may not qualify if:
- Over 85 years old
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Pittsburghlead
- National Eye Institute (NEI)collaborator
Study Sites (1)
University of Pittsburgh
Pittsburgh, Pennsylvania, 15213, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Gadi Wollstein, MD
University of Pittsburgh
Study Design
- Study Type
- observational
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 19, 2006
First Posted
June 23, 2006
Study Start
October 1, 2004
Primary Completion
December 1, 2010
Study Completion
January 1, 2011
Last Updated
October 25, 2016
Record last verified: 2011-07