Ophthalmology
Volume 118, Issue 3 , Pages 459-467, March 2011

Randomized Evaluation of the Trabecular Micro-Bypass Stent with Phacoemulsification in Patients with Glaucoma and Cataract

Presented at: the American Academy of Ophthalmology 2009 Annual meeting, October 2009, San Francisco, California; and in part at the American Society of Cataract and Refractive Surgery 2010 Annual Meeting, April 2010, Boston, Massachusetts.

  • Thomas W. Samuelson, MD

      Affiliations

    • Minnesota Eye Consultants, Minneapolis, Minnesota
  • ,
  • L. Jay Katz, MD

      Affiliations

    • Wills Eye Hospital, Philadelphia, Pennsylvania
  • ,
  • Jeffrey M. Wells, PharmD

      Affiliations

    • Glaukos Corporation, Laguna Hills, California
  • ,
  • Yi-Jing Duh, PhD

      Affiliations

    • ClinReg Consulting, Inc., Laguna Beach, California
  • ,
  • Jane Ellen Giamporcaro, BS

      Affiliations

    • Glaukos Corporation, Laguna Hills, California
    • Corresponding Author InformationCorrespondence: Jane Ellen Giamporcaro, BS, Glaukos Corp., 26051 Merit Circle #103, Laguna Hills, CA 92653
  • ,
  • US iStent Study Group

Received 19 December 2009; received in revised form 1 July 2010; accepted 7 July 2010. published online 09 September 2010.

Available online: September 15, 2010.

Objective

To assess the safety and efficacy of the iStent trabecular micro-bypass stent (Glaukos Corporation, Laguna Hills, CA) in combination with cataract surgery in subjects with mild to moderate open-angle glaucoma.

Design

Prospective, randomized, open-label, controlled, multicenter clinical trial.

Participants

A total of 240 eyes with mild to moderate open-angle glaucoma with intraocular pressure (IOP) ≤24 mmHg controlled on 1 to 3 medications were randomized to undergo cataract surgery with iStent implantation (treatment group) or cataract surgery only (control). Fifty additional subjects were enrolled to undergo cataract surgery with iStent implantation under protocol expansion. Data in this report are based on the first 240 eyes enrolled.

Intervention

Implantation of the iStent trabecular micro-bypass stent in conjunction with cataract surgery or cataract surgery only.

Main Outcome Measures

The primary efficacy measure was unmedicated IOP ≤21 mmHg at 1 year. A secondary measure was unmedicated IOP reduction ≥20% at 1 year. Safety measures included best-corrected visual acuity (BCVA), slit-lamp observations, complications, and adverse events.

Results

The study met the primary outcome, with 72% of treatment eyes versus 50% of control eyes achieving the criterion (P<0.001). At 1 year, IOP in both treatment groups was statistically significantly lower from baseline values. Sixty-six percent of treatment eyes versus 48% of control eyes achieved ≥20% IOP reduction without medication (P = 0.003). The overall incidence of adverse events was similar between groups with no unanticipated adverse device effects.

Conclusions

Pressure reduction on fewer medications was clinically and statistically significantly better 1 year after stent plus cataract surgery versus cataract surgery alone, with an overall safety profile similar to that of cataract surgery alone.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found after the references.

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 Manuscript no. 2009-1734.

 Financial Disclosure(s): The author(s) have made the following disclosure(s): TWS: C, O to Glaukos, and C to Alcon, Allergan, AMO, AqueSys, iScience, Ivantis, Pfizer, QLT, and Santen. LJK: C, O to Glaukos, C to Allergan, Alcon, Pfizer, and Lumenis; JW: E, O to Glaukos; Y-JD: C, O to Glaukos and C to Ivantis; JEG: E, O to Glaukos. All the investigators were consultants to Glaukos for the conduct of this study. In addition, Drs. Bacharach, Buznego, Cantor, and Nichamin are equity owners of Glaukos.

 Funding: Glaukos Corp.

 This study was registered with clinicaltrials.gov as NCT00323284.

PII: S0161-6420(10)00743-8

doi:10.1016/j.ophtha.2010.07.007

Ophthalmology
Volume 118, Issue 3 , Pages 459-467, March 2011