Overview
Pain Reduction With Topical Bromfenac Versus Artificial Tear After Intravitreal Injection.
Status:
Completed
Completed
Trial end date:
2023-11-15
2023-11-15
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this prospective interventional study is to compare post-intravitreal injection pain between eyes receiving topical bromfenac versus artificial tears as an analgesic after intravitreal injection.Phase:
Phase 4Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Wills EyeTreatments:
Bromfenac
Lubricant Eye Drops
Criteria
Inclusion criteria are:- Current patient of the Wills Eye Hospital Retina Service including all Mid Atlantic
Retina offices
- Clinical indication of bilateral intravitreal anti-vascular endothelial growth factor
(VEGF) injection as determined by the treating retina specialist for diseases such as
age-related macular degeneration, choroidal neovascularization, diabetic macular
edema, diabetic retinopathy, macular edema. proliferative retinopathy, or macular
edema associated with retina vein occlusion.
- Age greater than 18
- Patient's that have had at least three prior injections in each eye
Exclusion criteria are:
- Prior ocular surgery (non-cataract)
- Herpetic eye disease
- Uncontrolled uveitis
- Active conjunctivitis, keratitis or keratopathy
- Current unilateral use of prescription eye drops.
- Allergy to NSAID