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Osteoporosis Research Registry

Sponsor
Northwestern University (Other)
Overall Status
Completed
CT.gov ID
NCT01223300
Collaborator
Shirley Ryan AbilityLab (Other)
12
Enrollment
1
Location
97
Duration (Months)
0.1
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The aim of this research registry is to collect information on individuals with osteoporosis, those with risk factors for osteoporosis, and comparative healthy controls. Bone mineral density measurements will be done on these individuals to determine bone health.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The goal of this project is to develop a registry of research subjects with OP, with a risk of developing OP, and healthy controls. DXA scans will be performed on willing individuals at the spine, hips, and forearms and possibly the legs and heels in order to determine BMD. Subjects will also be asked to provide two (10 ml) blood samples, which may be used to analyze Vitamin D levels and/or other bone markers. By participating in the registry, subjects will be considered for current and future clinical research studies.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    12 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    Osteoporosis Research Registry
    Study Start Date :
    Nov 1, 2008
    Actual Primary Completion Date :
    Dec 1, 2016
    Actual Study Completion Date :
    Dec 1, 2016

    Arms and Interventions

    Arm Intervention/Treatment
    Osteoporosis

    Outcome Measures

    Primary Outcome Measures

    1. BMD [0 months]

    Secondary Outcome Measures

    1. Bone markers [0 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Any subjects who give written informed consent
    Exclusion Criteria:
    • Any individual who is not willing or able to give written informed consent

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Northwestern University Feinberg School of Medicine Chicago Illinois United States 60611

    Sponsors and Collaborators

    • Northwestern University
    • Shirley Ryan AbilityLab

    Investigators

    • Principal Investigator: Thomas J Schnizter, M.D., PhD, Northwestern University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Thomas J. Schnitzer, professor, Northwestern University
    ClinicalTrials.gov Identifier:
    NCT01223300
    Other Study ID Numbers:
    • STU00007523
    First Posted:
    Oct 18, 2010
    Last Update Posted:
    Dec 19, 2016
    Last Verified:
    Dec 1, 2016
    Additional relevant MeSH terms:
    Osteoporosis

    Study Results

    No Results Posted as of Dec 19, 2016