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Randomized Trial of Beta-Carotene and Macular Degeneration

Primary Purpose

Macular Degeneration

Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Aspirin
Beta-Carotene
Sponsored by
National Eye Institute (NEI)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Macular Degeneration focused on measuring Age-Related Macular Degeneration

Eligibility Criteria

40 Years - 84 Years (Adult, Older Adult)MaleAccepts Healthy Volunteers

When the Physicians Health Study was established in the early 1980s by the NHLBI to collect data on a stable population at risk for heart attack, only male physicians were studied because males were thought to be at higher risk than females for ischemic heart problems. The study population consists of 22,071 male U.S. physicians who were aged 40 to 84 years in 1982. The subjects have no history of myocardial infarction, cancer, kidney disease, renal disease, or any other contraindication to the use of aspirin or beta-carotene, including regular use of corticosteroids.

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Secondary Outcome Measures

    Full Information

    First Posted
    September 23, 1999
    Last Updated
    June 23, 2005
    Sponsor
    National Eye Institute (NEI)
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00000152
    Brief Title
    Randomized Trial of Beta-Carotene and Macular Degeneration
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2001
    Overall Recruitment Status
    Unknown status
    Study Start Date
    April 1982 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Name of the Sponsor
    National Eye Institute (NEI)

    4. Oversight

    5. Study Description

    Brief Summary
    To determine whether 50 mg of beta-carotene taken every other day reduces the risk of developing age-related macular degeneration (AMD) among male U.S. physicians who were aged 40 to 84 in 1982. To investigate the possible relationship of AMD with other antioxidants, including selenium and vitamins A, C, and E. To identify potential risk factors for development of AMD. Possible risk factors include height, systemic hypertension, cardiovascular disease, blood cholesterol, cigarette smoking, iris and skin color, sunlight exposure, body mass index, diabetes, and alcohol intake.
    Detailed Description
    Macular degeneration, a major cause of blindness in the United States, is the leading cause of new cases of blindness in people aged 65 and older. The National Eye Institute estimates that each year an additional 165,000 people, mainly in the older age groups, develop macular disease. Among all people with macular degeneration, approximately 116,000 are affected by the neovascular form of the disease. Although laser treatment is an effective treatment for patients with certain forms of neovascular membranes (exudative AMD), for most patients there is no available treatment. The pathogenesis of AMD is only partly understood, and its etiology remains obscure. The Retinal and Choroidal Diseases Panel of the National Advisory Eye Council has stated that "none of the fundamental causes of any type of macular disease is known, and none can be prevented." Thus, this panel recommended that one of the NEI's program development priorities should be to "initiate epidemiologic studies of macular diseases to identify possible causative, protective, or aggravating factors." This trial is part of the Physicians Health Study, sponsored by the National Heart, Lung, and Blood Institute (NHLBI) of the National Institutes of Health, with funding for eye epidemiologic data evaluations provided by the NEI. It is an ongoing, randomized, placebo-controlled trial of aspirin in the prevention of cardiovascular mortality and of beta-carotene in the prevention of cancer. Following randomization, each of the 22,071 physicians enrolled was assigned to one of four groups to take either aspirin or its placebo and beta-carotene or its placebo. Followup questionnaires are sent 6 and 12 months after randomization and every 12 months thereafter. The average length of followup is now greater than 12 years. The hypothesis that beta-carotene levels are inversely related to AMD is supported by experimental studies on the relationship between antioxidants and retinal morphology and function. There is increasing evidence that visible and ultraviolet light can damage the retina through production of superoxide radicals. Antioxidants (including beta-carotene, vitamins A, E, and C, and selenium) protect against oxidative damage by acting as scavengers for the superoxide radicals. Epidemiologic data from the first National Health and Nutrition Examination Survey (NHANES-1) are also consistent with a link between antioxidants and AMD; the frequency of consumption of fruits and vegetables rich in vitamin A (beta-carotene) was negatively correlated with AMD after adjustment for demographic and medical factors. Data from this study will determine whether one 50-mg beta-carotene capsule taken on alternate days protects against the development of AMD and whether additional risk factors emerge after simultaneous controlling for other potential confounding factors. Reported diagnoses of AMD are confirmed by medical record review. The primary analysis will be a comparison of incidence of reported AMD in the beta-carotene and placebo groups. The Cox proportional hazards model will also be used to determine whether there is a difference in time to diagnosis of AMD between the two groups.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Macular Degeneration
    Keywords
    Age-Related Macular Degeneration

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 3
    Allocation
    Randomized

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    Aspirin
    Intervention Type
    Drug
    Intervention Name(s)
    Beta-Carotene

    10. Eligibility

    Sex
    Male
    Minimum Age & Unit of Time
    40 Years
    Maximum Age & Unit of Time
    84 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    When the Physicians Health Study was established in the early 1980s by the NHLBI to collect data on a stable population at risk for heart attack, only male physicians were studied because males were thought to be at higher risk than females for ischemic heart problems. The study population consists of 22,071 male U.S. physicians who were aged 40 to 84 years in 1982. The subjects have no history of myocardial infarction, cancer, kidney disease, renal disease, or any other contraindication to the use of aspirin or beta-carotene, including regular use of corticosteroids.

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    17353403
    Citation
    Christen WG, Manson JE, Glynn RJ, Gaziano JM, Chew EY, Buring JE, Hennekens CH. Beta carotene supplementation and age-related maculopathy in a randomized trial of US physicians. Arch Ophthalmol. 2007 Mar;125(3):333-9. doi: 10.1001/archopht.125.3.333.
    Results Reference
    derived

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    Randomized Trial of Beta-Carotene and Macular Degeneration

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