Prevalence of Osteoporosis in Korean Prostate Cancer Patients Who is Receiving LHRH Agonist and/or Anti-androgen Agent

Sponsor
AstraZeneca (Industry)
Overall Status
Completed
CT.gov ID
NCT01025479
Collaborator
(none)
829
18
3.9
46.1
11.7

Study Details

Study Description

Brief Summary

Prevalence rate of osteoporosis and it's actual management condition in Prostate cancer patients who takes LHRH antagonist and anti androgen

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    829 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Retrospective
    Official Title:
    Prevalence of Osteoporosis in Korean Prostate Cancer Patients Who is Receiving LHRH Agonist and/or Anti-androgen Agent
    Study Start Date :
    Nov 1, 2009
    Actual Primary Completion Date :
    Mar 1, 2010
    Actual Study Completion Date :
    Mar 1, 2010

    Outcome Measures

    Primary Outcome Measures

    1. To define prevalence rate of osteoporosis in Prostate cancer patients who take LHRH antagonist or anti androgen (include MAB) at the stage of before treatment or it's initial stage. []

    Secondary Outcome Measures

    1. To assess whether proper osteoporosis prevention and treatment was given or not according to osteoporosis treatment guideline in prostate cancer patients who are enrolled in this study. []

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • pathologic confirmation of prostate cancer

    • patients who are taking LHRH antagonist or anti- androgen or both of them within 6 months since starting.

    Exclusion Criteria:
    • patients who are hard to be analysed by limitation of chart record according to investigators'discretion

    • patients who already have been registered in this study

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Research Site Cheongju-si Chungcheongbuk-do Korea, Republic of
    2 Research Site Chungju-si Chungcheongbuk-do Korea, Republic of
    3 Research Site Cheonan-si Chungcheongnam-do Korea, Republic of
    4 Research Site Gangneung-si Gangwon-do Korea, Republic of
    5 Research Site Goyang-si Gyeonggi-do Korea, Republic of
    6 Research Site Guri-si Gyeonggi-do Korea, Republic of
    7 Research Site Gumi-si Gyeongsangbuk-do Korea, Republic of
    8 Research Site Gyeongju-si Gyeongsangbuk-do Korea, Republic of
    9 Research Site Masan-si Gyeongsangnam-do Korea, Republic of
    10 Research Site Iksan-si Jeollabuk-do Korea, Republic of
    11 Research Site Daegu Korea, Republic of
    12 Research Site Daejeon Korea, Republic of
    13 Research Site Gwangju Korea, Republic of
    14 Research Site Incheon Korea, Republic of
    15 Research Site Jeju Korea, Republic of
    16 Research Site Pusan Korea, Republic of
    17 Research Site Seoul Korea, Republic of
    18 Research Site Ulsan Korea, Republic of

    Sponsors and Collaborators

    • AstraZeneca

    Investigators

    • Study Director: Joon Woo Bahn, MD, AstraZeneca Korea

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT01025479
    Other Study ID Numbers:
    • NIS-OKR-CAS-2009/1
    First Posted:
    Dec 3, 2009
    Last Update Posted:
    Jun 30, 2010
    Last Verified:
    Jun 1, 2010

    Study Results

    No Results Posted as of Jun 30, 2010