Diabetic Macular Edema Clinical Trial
Official title:
A Phase I Dose Ranging Study Evaluating the Safety and Efficacy of Cooling Anesthesia for Local Anesthesia During Intravitreal Injection (COOL 1)
The purpose of this clinical study is to evaluate the safety and efficacy of cooling anesthesia application to the eye as anesthesia for intravitreal injection using a novel cooling anesthesia device and determine the effects of temperature and duration of application on subjective pain after intravitreal injection.
Intravitreal injections have become the standard of care for administering medications for
retinal diseases such as age related macular degeneration and diabetic macular edema. There
is considerable apprehension among patients receiving these injections, primarily revolving
around adequate anesthesia during the injection. Current methods of anesthesia involve
topical anesthetic drops, lidocaine gels, or subconjunctival injections of lidocaine, which
suffer from either poor anesthetic effect, corneal irritation, or subconjunctival hemorrhage,
as well as significant time for the onset of anesthesia.
Recens Medical has developed a novel medical device which can precisely and rapidly cool the
surface of the eye This device cools to a temperature around -5 to -10 degrees Celsius, about
the temperature of a cold ice cube, and thus has an excellent safety profile compared to
conventional ophthalmic cryotherapy units. The value of such a device is both improved
patient comfort, as well as increased efficiency and workflow for retina specialists
administering intravitreal injections.
This device has been extensively tested in animal safety studies as well as pilot human
studies and has not demonstrated any serious adverse effects and has shown anesthetic effects
comparable to current standard of care.
This dose escalation study will test various temperatures and duration of temperatures to
evaluate for safety as well as determine the optimal temperature for anesthesia during
intravitreal injection.
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