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Comparison of Bone Effects With Copaxone and Interferon in Multiple Sclerosis: A Pilot Study
The purpose of this study is to determine if certain drugs commonly used to treat multiple sclerosis have an effect on bone health.
There will be 60 female patients with MS at University of Kansas Medical Center (KUMC). They will be split into two groups: a Copaxone group and an Interferon (Avonex, Rebif, or Betaseron) group. Each group will be composed of 30 women matched for menopausal status. Each subject will be given a questionnaire assessing risk factors for low bone density. All patients will have a determination of an Expanded Disability Status Scale (EDSS), height and weight, medical history, and fracture history. All patients will undergo hip and spine dual x-ray absorptiometry (DEXA) and will have labs drawn to determine serum 25 hydroxyvitamin D, parathyroid hormone, ionized calcium, estradiol, bone-specific acetyl phosphatase, osteocalcin, and C-peptides.
Age
18 - No limit years
Sex
FEMALE
Healthy Volunteers
No
General Clinical Research Center
Kansas City, Kansas, United States
University of Kansas Medical Center
Kansas City, Kansas, United States
Start Date
June 1, 2007
Primary Completion Date
February 1, 2009
Completion Date
December 1, 2012
Last Updated
January 22, 2014
60
ACTUAL participants
Copaxone
DRUG
Interferon-beta 1a
DRUG
Interferon-beta 1b
DRUG
Lead Sponsor
Nancy Hammond, MD
Collaborators
NCT06276634
NCT07225504
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06809192