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Clinical trialNCT00119535CompletedInterventional

Study to Evaluate the Effectiveness of a Program Developed to Improve Eye Care for Veterans With Diabetes

SponsorUS Department of Veterans AffairsEnrollment2,000Diabetes MellitusDiabetic Retinopathy
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The study's primary objective is to determine whether the PRSS improves the optimal timing of photocoagulation in diabetic patients in VA. Secondary objectives include assessing if the program: (1) leads to improved compliance with retinopathy screening and surveillance visits; (2) improves patient and provider satisfaction with VA diabetic eye care; (3) reduces eye care visit rates among diabetics receiving eye care at VA; (4) decreases health care resource utilization; and (5) improves the cost-effectiveness of eye care for patients with diabetes

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

  • Rodney A. Hayward, MD

    VA Ann Arbor Healthcare System, Ann Arbor, MI

    Principal Investigator
  • Steven J. Bernstein, MD MPH

    VA Ann Arbor Healthcare System, Ann Arbor, MI

    Principal Investigator

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

3 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Va Greater Los Angeles Healthcare System, West Los Angeles, Ca

    West Los Angeles, California, United States

  • Va Ann Arbor Healthcare System, Ann Arbor, Mi

    Ann Arbor, Michigan, United States

  • Louis Stokes Va Medical Center, Cleveland, Oh

    Cleveland, Ohio, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Aug 2004
Primary completion
—
Completion
31 Dec 2005
Last update posted
7 Apr 2015
Registered enrollment
2,000
Registry id
NCT00119535

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 11 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.