Analysis of Biomarkers From Patients With Chorioretinal Diseases
1 other identifier
observational
100
1 country
1
Brief Summary
This study was conducted to investigate the levels of ocular biomarkers from the patients with chorioretinal diseases including diabetic retinopathy, retinal vascular diseases, age-related macular degeneration (dry and wet), and retinal degeneration.
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 Apr 2012
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
April 1, 2012
CompletedFirst Submitted
Initial submission to the registry
December 29, 2013
CompletedFirst Posted
Study publicly available on registry
January 3, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
April 1, 2031
March 6, 2025
March 1, 2025
15.8 years
December 29, 2013
March 3, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Biomarkers in ocular fluids
To establish if certain type of chorioretinal diseases group are associated to different concentrations of gene or protein concentration.
one month
Study Arms (2)
Chorioretinal diseases
chorioretinal diseases including diabetic retinopathy, retinal vascular diseases, age-related macular degeneration (dry and wet), and retinal degeneration.
Control
control patients with surgeries include pars plana vitrectomy of macular hole, epiretinal membrane, cataract surgery.
Interventions
chorioretinal diseases including diabetic retinopathy, retinal vascular diseases, age-related macular degeneration (dry and wet), and retinal degeneration
Eligibility Criteria
A total of 100 patients will be included. 50 patients with chorioretinal diseases including diabetic retinopathy, retinal vascular diseases, age-related macular degeneration (dry and wet), and retinal degeneration. and 50 control patients scheduled for pars plana vitrectomy for nondiabetic retinal disease or phacoemulsification.
You may qualify if:
- age over 20 years
- patients requiring ophthalmologic treatments for different degrees of decreasing of visual acuity.
- patients with chorioretinal diseases including diabetic retinopathy, retinal vascular diseases, age-related macular degeneration (dry and wet), and retinal degeneration.
- control patients asking cataract surgery or vitrectomy for posterior segment nonproliferative disorders.
You may not qualify if:
- under the age of 20 years
- patients that received any anti-vascular endothelial growth factor agent for proliferative disease before taking sample of aqueous humor
- patients that did not signed the informed consent of the trial
- patients with intraocular inflammations or infections that requiring any pharmaceutical agent
- patients with recent ocular trauma
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Dong Ho Park
Daegu, Kyungsangpookdo, 700-721, South Korea
Biospecimen
certain gene or protein levels in ocular fluid
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Dong Ho Park, M.D
Kyungpook National University Hospital
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Department of Opthalmology, School of medicine, Kyungpook National University
Study Record Dates
First Submitted
December 29, 2013
First Posted
January 3, 2014
Study Start
April 1, 2012
Primary Completion (Estimated)
February 1, 2028
Study Completion (Estimated)
April 1, 2031
Last Updated
March 6, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will not share