Diagnostic Innovations in Glaucoma Study

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The overarching goal of our research study is to evaluate changes in visual function and optic nerve topography (the structure of the back of the eye) in patients with glaucoma (increased susceptibility to pressure inside the eye that can cause loss of vision) or those with an increased risk of developing the disease. The purpose of this study is to determine the best methods for detecting the presence or progression (worsening over time) of glaucoma in patients with and without myopia and its effects on daily and visual function and quality of life. With several sources of NIH and foundation funding over the last twenty years we have designed a robust research protocol to address the most challenging aspects of glaucoma management. The most recent focus of this research is 1) to improve our ability to detect open angle glaucoma in individuals with myopia and in individuals of European and African descent, 2) to determine whether monitoring of the retinal vasculature with new optical imaging instruments can improve glaucoma management and elucidate the pathophysiology of the disease, and 3) to differentiate between age-related changes and glaucomatous progression. The grants supporting this project include 3 NIH funded studies, 1) the University of California, San Diego UCSD -based Diagnostic Innovations in Glaucoma Study (DIGS funded since 1995): 2) the African Descent and Glaucoma Evaluation Study (ADAGES funded since 2002), 3) the Brightfocus Foundation National Glaucoma Research Program and 4) the UCSD-based Diagnosis and Monitoring of Glaucoma with Optical Coherence Tomography Angiography (funded since 2018). The ADAGES is a multi-center study with data collection also conducted at 2 other academic sites, the University of Alabama at Birmingham, and Columbia University. Enrolled healthy participants, glaucoma suspects and glaucoma patients are generally asked to return for two or more visits a year for several years. We then analyze whether the glaucoma patients are progressing and what factors influence their glaucoma status compared to healthy subjects and individuals suspected of having glaucoma.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Subjects are healthy controls with or without myopia, and patients with or without myopia with a diagnosis of glaucoma, glaucoma suspect and ocular hypertension

• They will be considered if they are above 18 years old.

• There is no upper age limit

• Subject are not restricted by gender, race or ethnicity.

Locations
United States
California
UCSD, Hamilton Glaucoma Center
RECRUITING
La Jolla
Contact Information
Primary
Veronica Inpirom
vrubio@health.ucsd.edu
858-822-4669
Time Frame
Start Date: 1995-04
Estimated Completion Date: 2030-07
Participants
Target number of participants: 3000
Treatments
Healthy individuals
healthy controls with or without myopia
Persons at risk for or with primary open angle glaucoma
with or without myopia with a diagnosis of glaucoma, glaucoma suspect and ocular hypertension
Sponsors
Collaborators: National Eye Institute (NEI)
Leads: University of California, San Diego

This content was sourced from clinicaltrials.gov