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Calcium DXA: Impact of Calcium Supplements on Lumbar Spine Bone Mineral Density

This study has been completed.

Sponsored by: University of Wisconsin, Madison
Information provided by: University of Wisconsin, Madison
ClinicalTrials.gov Identifier: NCT00205036
  Purpose

We, the investigators at the University of Wisconsin, hypothesized that ingesting calcium tablets prior to a spine bone density scan will not affect the bone mineral density as measured by dual energy x-ray absorptiometry (DXA).


Condition
Healthy

MedlinePlus related topics:   Dietary Supplements    Minerals   

ChemIDplus related topics:   Calcium gluconate   

U.S. FDA Resources

Study Type:   Observational
Study Design:   Prospective
Official Title:   Impact of Calcium Supplements on Lumbar Spine Bone Mineral Density

Further study details as provided by University of Wisconsin, Madison:

Study Start Date:   January 2005

Detailed Description:

We hypothesized that ingesting calcium tablets prior to a spine bone density scan will not affect the bone mineral density as measured by DXA. To test this, 36 subjects ingested various calcium supplements after a spine DXA scan and were then scanned again 15, 30 and 45 minutes after ingestion. Subsequently a subset of 15 subjects had three spine scans performed for instrument precision and subsequently ingested a calcium tablet with scans 15 and 30 minute intervals after ingestion.

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria:

  • Men or women 18 years or older

Exclusion Criteria:

  • Internal spinal hardware
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00205036

Locations
United States, Wisconsin
University of Wisconsin    
      Madison, Wisconsin, United States, 53792

Sponsors and Collaborators
University of Wisconsin, Madison

Investigators
Principal Investigator:     Neil C Binkley, MD     University of Wisconsin, Madison    
  More Information


Responsible Party:   University of Wisconsin ( Neil Binkley, MD )
Study ID Numbers:   M2004-1308
First Received:   September 13, 2005
Last Updated:   December 26, 2007
ClinicalTrials.gov Identifier:   NCT00205036
Health Authority:   United States: Institutional Review Board

Study placed in the following topic categories:
Healthy

ClinicalTrials.gov processed this record on October 16, 2008




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