Overview
Analysis of Aqueous and Vitreous Humor
Status:
Unknown status
Unknown status
Trial end date:
2017-07-01
2017-07-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
Clinical Retina research studies often collect aqueous samples in hopes of estimating levels of drug or cytokines in the vitreous. Little is known about how well vitreous and aqueous correlate. This study will collect vitreous and aqueous samples at the same time to evaluate and compare drug and cytokine levels. The overall objective of this study is to evaluate the molecular concentration of growth factors, cytokines and chemokines in human aqueous humor and vitreous samples collected from individuals undergoing pars plana vitrectomy for tractional retinal detachment secondary to proliferative diabetic retinopathy, exudative or tractional retinal detachment secondary to macular degeneration, macular hole or neovascular glaucoma.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
California Retina ConsultantsTreatments:
Ranibizumab
Criteria
Inclusion Criteria:- Ability to provide written informed consent and comply with study assessments for the
full duration of the study
- Age > 18 years
- Subjects with a diagnosis of tractional retinal detachment secondary to proliferative
diabetic retinopathy, age-related macular degeneration with tractional or exudative
retinal detachment, macular hole, epiretinal membrane, or neovascular glaucoma.
Exclusion Criteria:
- Subjects with history of vitrectomy in the study eye
- Presence of vitreous hemorrhage
- Subjects with history of laser photocoagulation in the study eye within 3 months of
vitrectomy
- Subjects unwilling to undergo pars plana vitrectomy
- Subjects unwilling to receive intravitreal ranibizumab prior to pars plana vitrectomy
unless diagnosis of macular hole or epiretinal membrane
- Subjects who may need or have received systemic anti-VEGF for oncology in the past
year
- Subjects with history of anti-VEGF injection within 4 months before vitrectomy