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Absorption and Distribution of Glucosamine and Chondroitin
This study has been completed.
Study NCT00086229   Information provided by National Center for Complementary and Alternative Medicine (NCCAM)
First Received: June 28, 2004   Last Updated: August 16, 2006   History of Changes

June 28, 2004
August 16, 2006
April 2004
 
 
Complete list of historical versions of study NCT00086229 on ClinicalTrials.gov Archive Site
 
 
 
Absorption and Distribution of Glucosamine and Chondroitin
A Pharmacokinetic Study of Glucosamine and Chondroitin

The purpose of this study is to examine the way the dietary supplements glucosamine and chondroitin are absorbed and distributed throughout the body.

Osteoarthritis is the most common musculoskeletal disease in the world. While predisposing conditions have been identified, the actual cause of osteoarthritis remains unknown. Traditional treatments, most often anti-inflammatory drugs and pain relievers, produce variable results and may cause significant toxicity. The use of complementary and alternative therapies in the treatment of osteoarthritis has become more common, and particular interest has focused on glucosamine and chondroitin treatments. This study will examine the pharmacokinetics of glucosamine and chondroitin.

This study consists of two phases. In Phase I, participants will have two study visits, during which multiple blood samples will be taken to determine levels of glucosamine and chondroitin found naturally in the body.

During Phase II, participants will be randomly assigned to receive glucosamine, chondroitin, or a combination of the two for 3 months. Blood samples will be taken at each of the three Phase II study visits to examine the pharmacokinetics of glucosamaine and chondroitin.

 
Interventional
Treatment, Randomized, Open Label, Uncontrolled, Parallel Assignment, Pharmacokinetics Study
Osteoarthritis
  • Drug: Glucosamine
  • Drug: Chondroitin
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
70
January 2006
 

Inclusion Criteria:

  • Able to walk

Exclusion Criteria:

  • Allergy to glucosamine, chondroitin, or shellfish
  • Liver or kidney disease
  • Diabetes mellitus
  • Concurrent use of other complementary or alternative therapies
Both
21 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00086229
 
R21 AT001938-01
National Center for Complementary and Alternative Medicine (NCCAM)
 
Principal Investigator: Christopher G. Jackson, MD University of Utah
National Center for Complementary and Alternative Medicine (NCCAM)
August 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP