Pilot Study: A Randomized Trial Of Anesthetic Agents For Intravitreal Injection
Macular Degeneration
About this trial
This is an interventional treatment trial for Macular Degeneration focused on measuring Macular Degeneration, Intravitreal injections, Eye anesthesia-Topical/subconjunctival, Eye-surgical procedures, Ophthalmologic anesthesia methods
Eligibility Criteria
Inclusion Criteria:
- Male or female > 40 years of age
- Diagnosis of age-related macular degeneration
- History of at least 1 intravitreal injection in the past in either eye
- Written informed consent has been obtained
Exclusion Criteria:
- Known allergy or sensitivity to the study medications(s), it's components, or other agents required for the study procedures(e.g. Povidone iodine)
Sites / Locations
- Lahey Clinic Arlington
- Lahey Clinic, Inc.
- Lahey Clinic Northshore
Arms of the Study
Arm 1
Other
All Participants
All Participants will be randomized to receive a unique sequence of one of the 4 anesthetic agents per month, prior to a standard of care monthly intravitreal injection (1 injection per month for a total of 4 months). At the end of study participation, each patient will have received each of the 4 anesthetic agents once prior to one of the 4 intravitreal injections (ex. Randomization to sequence: Proparacaine Ophthalmic drops used prior to Injection 1; Tetracaine Ophthalmic drops used prior to Injection 2; Lidocaine 4% sponge used prior to Injection 3; Lidocaine 2% injectable solution (subconjunctival) used prior to Injection 4).