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NCT01223300 Clinical Trial

Osteoporosis Research Registry

Osteoporosis Clinical Trial

Official title:
Osteoporosis Research Registry

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01223300
Other study ID # STU00007523
Secondary ID
Status Completed
Phase N/A
First received October 14, 2010
Last updated December 16, 2016
Start date November 2008
Est. completion date December 2016

Study information
Verified date December 2016
Source Northwestern University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial 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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 12
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Any subjects who give written informed consent

Exclusion Criteria:

- Any individual who is not willing or able to give written informed consent

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Northwestern University Feinberg School of Medicine Chicago Illinois

Sponsors (2)
Lead Sponsor Collaborator
Northwestern University Rehabilitation Institute of Chicago

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary BMD 0 months No
Secondary Bone markers 0 months No
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