Clinical Trials

To determine the effectiveness of the ARTISAN Aphakia lens in the treatment of aphakia and to precisely define the associated risks and, if possible, identify particular groups of patients who may be at high risk of developing complications resulting from the surgical procedure of implanting an ARTISAN Aphakia lens.

The purpose of this study is to assess patient satisfaction differences, if any, with cataract surgery using the validated Iowa Satisfaction with Anesthesia Scale in patient groups undergoing either monitored anesthesia care or nurse sedation care.

The aim of this study is to assess if the doses of midazolam and fentanyl during a cataract procedure under topical anesthesia contributes to changes in overall patient satisfaction.

This study is being done to learn about cataract surgery in children. The study involves the collection of information about children who have had cataract surgery. This information will include when the child developed cataract, how the cataract has been treated, problems that may have occurred related to surgery, and whether anyone else in the family has had a cataract. Doctors throughout the United States and possibly other parts of the world are taking part in the study. We hope that gathering the information from many children we can improve the care of children with ...

The purpose of this study is to determine if patient satisfaction can be measured for cataract surgery under conscious sedation.

The purpose of this study is to analyze the rate of clinically relevant
complications associated with CyPass Micro-Stent (CyPass)
as determined at 36 months in patients with primary glaucoma undergoing cataract surgery.

The purpose of this study is to compare the safety and efficacy of goniotomy performed with a novel ophthalmic knife compared to trabecular bypass stent implantation in mild to moderate glaucoma subjects who are also undergoing cataract extraction with phacoemulsification (Phaco) and posterior chamber intraocular lens (PCIOL) implant.

The purpose of this study is to assess the safety of Dextenza compared to an active control, prednisolone acetate suspension, for the treatment of postoperative pain and inflammation following ocular surgery for pediatric cataract.

The objectives of this study are to determine if the 1-year graft success rate following DMEK performed with corneas from donors without diabetes is superior to the graft success rate with cornea donors with diabetes, to determine if the 1-year central endothelial cell loss (ECL) following DMEK performed with corneas from donors without diabetes is superior to the central ECL when corneas from donors with diabetes are used, nd to explore the relationship of severity of diabetes in the donor, as measured by eye bank-determined diabetes risk categorization scores, post-mortem hemoglobin A1c (HbA1c), and skin advanced glycation endproducts (AGE) and ...

This study is being done to:

- Assess what children with different eye conditions experience in everyday life

- Improve our understanding of the difficulties that children with eye problems experience

- Improve reporting of how parents see their child’s eye condition affecting them

- Assess what parents of children with different eye conditions experience in their own everyday life

- Improve the way we assess the benefits of treatment