Clinical Trials

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The physicians at Assil Gaur Eye Institute are dedicated to bringing innovative technology to our patients through clinical research and trials. These trials involve investigating leading-edge ophthalmic care, products, and devices.

 

Our clinical trials are carefully controlled research studies that gather scientific evidence to improve the ways we prevent, diagnose, or treat specific eye conditions. Each clinical study is led by one of our trusted medical doctors and our professional research team.

 

Many patients who have taken part in our clinical research trials have been helped as a result of having access to state-of-the-art care they otherwise would not have had. The first people to have been helped by medication or a medical device are often those who were part of its clinical trials.

Active Trials:
  • Recruiting Now

    ARTISAN® IOL (intraocular lens) Study

    Recruiting NOW
    Learn More
    Location:
    Beverly Hills
    Start Date:
    March, 2016
    End Date:
    TBD

    It is exciting to offer the ARTISAN® IOL to those patients who have a visually significant cataract, are aphakic or pseudophakic, and have compromised ocular anatomy that prohibits implantation of a standard posterior chamber IOL.

     

    The design of the ARTISAN lens is unique since it can be attached in front of the iris and does not require an intact or structurally sound capsular bag. While most patients will not qualify for this study as they will not need this specially designed lens, the Assil Gaur Eye Institute is fortunate to be one of just two study sites in California allowed to provide this as a potential solution for those patients where this is a beneficial option. (No health insurance is required.)

    Learn More
  • Recruiting Now

    OMNI® 2.0 Surgical System Clinical Study for Glaucoma Patients at AEI

    Recruiting NOW
    Learn More & Inquire
    Location:
    Beverly Hills
    Start Date:
    March, 2020
    End Date:
    TBD

    Assil Gaur Eye Institute is now enrolling patients in a multicenter, prospective post-market study utilizing the OMNI 2.0 (OMNI NextGen) Surgical System by Sight Sciences.

     

    This device is used in the management of glaucoma by aiding in lowering intraocular pressure. Specifically, for this study, individuals need to have a diagnosis of mild to moderate open angle glaucoma and have already had uncomplicated cataract surgery with implantation of a posterior chamber intraocular lens (IOL).

     

    Eligible patients enrolled in the trial will receive surgery for Open Angle Glaucoma using the OMNI® Surgical System. We are expecting and will be measuring for a decrease in unmedicated mean diurnal IOP (DIOP) and change in the number of ocular hypotensive medications at the between screening and 12-month postoperative visit.

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