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Efficacy of Surgical Systems in Combination With Phacoemulsification: a Retrospective Analysis

Sponsored by Barnet Dulaney Perkins Eye Centers

About this study

Real-World efficacy of Hydrus Microstent with OMNI Surgical System in combination with Phacoemulsification: a retrospective analysis

The use of combination Phacoemulsification, OMNI Canaloplasty and Hydrus microstent successfully lowers IOP in ethnically-diverse patients with Open Angle Glaucoma

Where this study is enrolling

Who can participate

Inclusion criteria

  • ✓Subjects with h/o CEIOL/OMNI/Hydrus (chosen based on subjects on more than 1 medication pre-operatively) with at least 3 years of follow up data
  • ✓have Glaucoma

Exclusion criteria

  • ✕Patients with angle closure glaucoma or secondary forms of glaucoma due to neovascularization of the angle, uveitic glaucoma, congenital glaucoma, or glaucoma due to congenital anomalies.
  • ✕Patients with refractory CME or CME persisting 3 months or more post-operatively
  • ✕Patients with incomplete IOP, medication logs or VF data within post-operative period
  • ✕Prior incisional surgery or MIGS

Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.

Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.

Trial data sourced from ClinicalTrials.gov.