Advanced Glaucoma Intervention Study (AGIS)

Sponsor
National Eye Institute (NEI) (NIH)
Overall Status
Unknown status
CT.gov ID
NCT00000148
Collaborator
(none)
13

Study Details

Study Description

Brief Summary

To assess the long-range outcomes of sequences of interventions involving trabeculectomy and argon laser trabeculoplasty in eyes that have failed initial medical treatment for glaucoma.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Argon Laser Trabeculoplasty
  • Procedure: Trabeculectomy
Phase 3

Detailed Description

In advanced glaucoma, medication alone no longer reduces intraocular pressure adequately, and the eye has field defects. Before 1980, some type of filtering surgery, such as trabeculectomy, was the usual method of intervention. Since then, laser trabeculoplasty has become a popular alternative. Sometimes the first intervention chosen succeeds in controlling pressure for many years; at other times, the success lasts only a few weeks or months. Because success is limited, some patients, over time, need to undergo a sequence of surgical interventions. Little is known about which sequence gives the best long-range outcome.

The Advanced Glaucoma Intervention Study (AGIS) is designed to provide a comprehensive assessment of the long-range outcomes of medical and surgical management in advanced glaucoma. The study uses visual function status to compare two intervention sequences in managing the disease.

Eligible eyes are randomly assigned to one of two intervention sequences: (1) trabeculectomy, followed by argon laser trabeculoplasty (ALT) should trabeculectomy fail, followed by a second trabeculectomy should ALT fail; or (2) ALT, followed by trabeculectomy should ALT fail, followed by another trabeculectomy should the first trabeculectomy fail. Antifibrotic agents may be used as an adjunct to trabeculectomy, but only in eyes with a previous history of invasive surgery. Eyes that fail the entire assigned sequence of interventions are managed at the discretion of the AGIS physician in collaboration with the patient.

Interventions are supplemented with medical treatment as needed. A total of 789 eyes with advanced glaucoma have been enrolled. All patients are being followed under a standardized protocol for a minimum of 5 years to determine degree of visual function loss, failure rates of interventions, rates of complications, and need for supplemental therapy.

After the initial intervention, followup examinations are scheduled at 1 week, 4 weeks, 3 months, 6 months, and every 6 months thereafter. After second and third interventions, followup examinations are scheduled at 1 and 4 weeks. Additional visits are scheduled as necessary for the management of the disease.

The primary outcome variable in AGIS is average percent of eyes with decrease of vision, where decrease of vision is a substantial decline of either visual field or visual acuity attributable to the effect of glaucoma. Secondary outcome variables include sustained decrease of vision, failure of interventions, number of prescribed glaucoma medications, and level of intraocular pressure. An ancillary study is assessing filtering bleb encapsulation.

Study Design

Study Type:
Interventional
Allocation:
Randomized
Primary Purpose:
Treatment
Study Start Date :
Apr 1, 1988

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    35 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Men and women between the ages of 35 and 80 with open-angle glaucoma that was not successfully controlled by medication were eligible for enrollment.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Yale University School of Medicine, Yale Eye Center New Haven Connecticut United States
    2 Georgetown University, University Ophthalmic Consultants of Washington, Eye Associates of Washington, D.C. Washington District of Columbia United States
    3 Emory University, Emory Eye Center Atlanta Georgia United States
    4 Piedmont Hospital, Eye Consultants of Atlanta Atlanta Georgia United States
    5 Humana Health Plan Sykes Center Chicago Illinois United States
    6 University of Illinois, Eye and Ear Infirmary Chicago Illinois United States
    7 Washington Hospital Center, Washington Eye Physicians and Surgeons Chevy Chase Maryland United States
    8 University of Michigan, W.K. Kellogg Eye Center Ann Arbor Michigan United States
    9 Sinai Hospital, Detroit, Franklin Eye Consultants Southfield Michigan United States
    10 Ohio State University, Department of Ophthalmology, Ophthalmic Surgeons and Consultants Columbus Ohio United States
    11 Wills Eye Hospital, Glaucoma Service Philadelphia Pennsylvania United States
    12 University of Virginia Medical Center, Department of Ophthalmology Charlottesville Virginia United States
    13 Medical College of Virginia, Department of Ophthalmology Richmond Virginia United States

    Sponsors and Collaborators

    • National Eye Institute (NEI)

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00000148
    Other Study ID Numbers:
    • NEI-49
    First Posted:
    Sep 24, 1999
    Last Update Posted:
    Jun 5, 2006
    Last Verified:
    Oct 1, 2003
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 5, 2006