Effect of Vascular Endothelial Growth Factor Blockers on Aqueous Humor Dynamics

Status: Terminated
Location: See all (2) locations...
Study Type: Observational
SUMMARY

The objective of this research is to determine the effects of anti-VEGF drugs (bevacizumab, ranibizumab or aflibercept) on aqueous humor dynamics (AHD) in patients with retinal vascular disease. The underlying hypothesis is that anti-VEGF drugs increase intraocular pressure (IOP) by increasing aqueous inflow, decreasing uveoscleral outflow or both. The specific aim is to evaluate the changes produced in AHD after 1 baseline and a subsequent 1 monthly injection of anti VEGF agents.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 19
Healthy Volunteers: f
View:

• Subjects must be at least 19 years of age and older

• Ability to give informed consent and attend the study visits

• Patients with established diagnosis of retinal vascular diseases (diabetic macular edema, neovascular macular degeneration,presumed ocular histoplasmosis syndrome, high myopia) who require intravitreal injection of anti-VEGF drugs such as bevacizumab,ranibizumab or aflibercept and are likely to need three monthly doses.

• Patients who have not received intravitreal injections within 3 months of study entry

• No previous established diagnosis of glaucoma and consequently no previous history of Argon Laser Trabeculoplasty (ALT) or Selective Laser Trabeculoplasty (SLT).

• No previous history of ocular surgery

• Patients who are not planning on and are unlikely to require an elective ocular surgical or laser procedure within the study duration

• Open angle of the anterior chamber on clinical examination

• Ability to cooperate for aqueous humor dynamic studies

• Contact lenses removed prior to topical fluorescein instillation, and not used until the end of each fluorophotometry session

• Able to participate on site over the multi-visit study period

Locations
United States
Nebraska
University of Nebraska Medical Center, Department of Ophthalmology and Visual Sciences
Omaha
University of Nebraska Medical Center, Truhlsen Eye Institute
Omaha
Time Frame
Start Date: 2013-12-20
Completion Date: 2023-01-12
Participants
Target number of participants: 13
Sponsors
Leads: University of Nebraska

This content was sourced from clinicaltrials.gov

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