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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00593437
Other study ID # 2006-1053
Secondary ID
Status Completed
Phase N/A
First received January 3, 2008
Last updated October 1, 2015
Start date February 2006
Est. completion date December 2006

Study information

Verified date April 2010
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Differences in determining bone density scores have been found when comparing different bone density machines. Reducing differences between machines will improve diagnostic agreement for patients measured at different clinics. This study will test if this difference exists between the Norland Excel, such as the one at Wildwood Clinic, and the GE Healthcare Lunar Prodigy at the UW Osteoporosis Clinical Research Center.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date December 2006
Est. primary completion date December 2006
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 40 Years and older
Eligibility Inclusion Criteria:

- Ambulatory women age 40 years and older

- Recent spine and hip DXA at Wildwood clinic in Madison, WI

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Wisconsin Osteoporosis Clinical and Research Program Madison Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Spine and hip BMD and T-score measurements will be compared between densitometry machines. 2 weeks No
See also
  Status Clinical Trial Phase
Enrolling by invitation NCT06151353 - Performance of REMS Bone Densitometry in a British Population