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Physicians' Health Study: Study of Low Cardiovascular Disease Mortality

Primary Purpose

Cardiovascular Diseases, Heart Diseases, Coronary Disease

Status
Completed
Phase
Locations
Study Type
Observational
Intervention
Sponsored by
National Heart, Lung, and Blood Institute (NHLBI)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an observational trial for Cardiovascular Diseases

Eligibility Criteria

undefined - 100 Years (Child, Adult, Older Adult)MaleDoes not accept healthy volunteers

No eligibility criteria

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Secondary Outcome Measures

    Full Information

    First Posted
    May 25, 2000
    Last Updated
    March 15, 2016
    Sponsor
    National Heart, Lung, and Blood Institute (NHLBI)
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00005252
    Brief Title
    Physicians' Health Study: Study of Low Cardiovascular Disease Mortality
    Study Type
    Observational

    2. Study Status

    Record Verification Date
    August 2004
    Overall Recruitment Status
    Completed
    Study Start Date
    January 1990 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    December 1992 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    National Heart, Lung, and Blood Institute (NHLBI)

    4. Oversight

    5. Study Description

    Brief Summary
    To explain the extremely low cardiovascular mortality among Physicians' Health Study (PHS) participants by ascertaining all cardiovascular and total deaths among the 90,457 physicians who returned enrollment forms but were not randomized into the study. Also, to compare the mortality experience of randomized physicians with various subgroups of non-participants.
    Detailed Description
    BACKGROUND: The Physicians' Health Study was a randomized, double-blind, placebo-controlled primary prevention trial designed to test whether 325 mg aspirin every other day reduced the risk of cardiovascular disease and whether 50 mg beta-carotene on alternate days decreased cancer incidence among 22,071 male physicians, aged 40-84 years in 1982. On December 18, 1987, the external Data Monitoring Board recommended early termination of the blinded aspirin component of the trial, based on the emergence of a statistically extreme benefit of aspirin on both fatal and nonfatal myocardial infarction, as well as the extraordinarily low cardiovascular mortality rates among study participants. DESIGN NARRATIVE: In January 1982, the Physicians' Health Study investigators purchased a tape from the American Medical Association that contained the names of all male physicians born between January 1, 1907 and December 31, 1942. The tape provided the basis for the invitation to join the trial. A new computer tape was purchased from the AMA that contained names, addresses, and dates of birth for all physicians registered as of December 1982, current and 1982 addresses, and any reported deaths. This tape was matched against Physician Health Study data files to eliminate those not on the original tape, as well as those known to be deceased at the time of the original mailing. When the match was complete, the results were a new tape that included names, most recent addresses, and dates of birth of all those who were invited to participate in the trial. A new master study tape was compiled that included all non-randomized potentially eligible respondents to the invitational mailing as well as a 35 percent random sample of the non-respondents. This group of 138,460 comprised the cohort. The National Death Index (NDI) was searched from January 1, 1982 to January 25, 1988, the official termination date of the trial for each physician in the cohort as well as for the 22,071 randomized participants. A copy of the death certificate was obtained from the state department of vital statistics for each death identified by the NDI in order to distinguish between vascular and non-vascular deaths. An Endpoints Committee, using death certificates and medical records in some cases, assigned the cause of death to be entered into the data base. Analyses were performed comparing: all randomized versus all non-randomized respondents; those randomized versus those eligible but unwilling to participate; those randomized versus those initially willing and eligible who enrolled in an 18 week period but were excluded prior to randomization. Baseline data on the enrollment forms were examined to determine whether differences in mortality rates could be explained by differences in cardiovascular risk factors among the groups. The study completion date listed in this record was obtained from the "End Date" entered in the Protocol Registration and Results System (PRS) record.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cardiovascular Diseases, Heart Diseases, Coronary Disease, Myocardial Infarction

    7. Study Design

    10. Eligibility

    Sex
    Male
    Maximum Age & Unit of Time
    100 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    No eligibility criteria
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Julie Buring
    Organizational Affiliation
    Brigham and Women's Hospital

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    1615847
    Citation
    Ridker PM, Manson JE, Goldhaber SZ, Hennekens CH, Buring JE. Comparison of delay times to hospital presentation for physicians and nonphysicians with acute myocardial infarction. Am J Cardiol. 1992 Jul 1;70(1):10-3. doi: 10.1016/0002-9149(92)91381-d.
    Results Reference
    background
    PubMed Identifier
    10636266
    Citation
    Gaziano JM, Gaziano TA, Glynn RJ, Sesso HD, Ajani UA, Stampfer MJ, Manson JE, Hennekens CH, Buring JE. Light-to-moderate alcohol consumption and mortality in the Physicians' Health Study enrollment cohort. J Am Coll Cardiol. 2000 Jan;35(1):96-105. doi: 10.1016/s0735-1097(99)00531-8.
    Results Reference
    background
    PubMed Identifier
    12600848
    Citation
    Liu S, Sesso HD, Manson JE, Willett WC, Buring JE. Is intake of breakfast cereals related to total and cause-specific mortality in men? Am J Clin Nutr. 2003 Mar;77(3):594-9. doi: 10.1093/ajcn/77.3.594.
    Results Reference
    background

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    Physicians' Health Study: Study of Low Cardiovascular Disease Mortality

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