Search and volunteer to participate in these available studies at UB. Your participation in research doesn't just benefit you, it helps advance healthcare for our entire community.
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Showing 1 - 7 of 7 Clinical Trials
Description:
This study enrolls people who need tube shunt implantation for the treatment of their severe glaucoma. The purpose of this study is to learn which type of tube shunt (a device used during the surgery) works the best. Read More
Eligibility:
Adults ages 18+.
Have significant uncontrolled glaucoma despite medical, laser or previous surgery that requires tube shunt implantation.
Are scheduled for glaucoma tube shunt implantation surgery.
Have significant uncontrolled glaucoma despite medical, laser or previous surgery that requires tube shunt implantation.
Are scheduled for glaucoma tube shunt implantation surgery.
Contact(s)
Description:
This study enrolls adults with Glaucoma who are scheduled for surgery. The purpose of this study is to learn the effects of varying the dose of the laser in a certain glaucoma surgical procedure (called MicroPulse Trans-Scleral CycloPhotoCoagulation). Read More
Eligibility:
-Adults ages 18+ who have been diagnosed with Glaucoma.
-People who have been invited to participate because they have been scheduled for MicroPulse Trans-Scleral CycloPhotoCoagulation (MP-TSCPC) surgery
-People who have been invited to participate because they have been scheduled for MicroPulse Trans-Scleral CycloPhotoCoagulation (MP-TSCPC) surgery
Contact(s)
Description:
We are looking for people with glaucoma and cataract in both eyes for this study. The purpose of the study is to compare two devices used in glaucoma surgery. Read More
Eligibility:
Adults ages 18+
Diagnosed with glaucoma in both eyes.
Needs glaucoma and cataract surgery.
Diagnosed with glaucoma in both eyes.
Needs glaucoma and cataract surgery.
Contact(s)
Description:
We are looking for children age 6-17 for this research study. The purpose of this study is to find out if the Spot Vision Screener is effective in measuring vision in this age group. Read More
Eligibility:
Age 6-17
Scheduled for a regular eye exam at the Ross Eye Institute
Contact(s)
Description:
This study enrolls children ages 4-13 who have amblyopia ("lazy eye"). The purpose of the study is to learn if vision is improved by playing a binocular game while wearing corrective glasses. Read More
Eligibility:
Children ages 4-13.
Diagnosed with amblyopia, also known as "lazy eye."
Diagnosed with amblyopia, also known as "lazy eye."
Contact(s)
Description:
This study enrolls newborn infants with treatable retinopathy of prematurity (ROP). ROP is is one of the leading causes of childhood blindness worldwide. The purpose of this study is to learn if aflibercept (Eyelea) works to treat this condition. Read More
Eligibility:
Children (newborn infants).
Gestational age at birth must be 32 weeks or less, birth weight must be 1500g or less
Must have retinopathy of prematurity (ROP) that has not yet been treated.
Must weigh at least 800 g
Gestational age at birth must be 32 weeks or less, birth weight must be 1500g or less
Must have retinopathy of prematurity (ROP) that has not yet been treated.
Must weigh at least 800 g
Contact(s)
Description:
This study enrolls children with myopia, or nearsightedness. The purpose of this study is to learn whether the use of SYD-101, an eye solution, slows down the progression of myopia in children. Read More
Eligibility:
-Children ages 3-14.
-Child must be in general good health.
-Must be diagnosed with myopia (nearsightedness) in both eyes.
-Child must be in general good health.
-Must be diagnosed with myopia (nearsightedness) in both eyes.
Contact(s)
Showing 1 - 7 of 7 Clinical Trials
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