Absorption and Distribution of Glucosamine and Chondroitin
This study is currently recruiting patients.
Verified by National Center for Complementary and Alternative Medicine (NCCAM) February 2005
Purpose
The purpose of this study is to examine the way the dietary supplements glucosamine and chondroitin are absorbed and distributed throughout the body.
| Condition |
Intervention |
Osteoarthritis
|
Drug: Glucosamine Drug: Chondroitin
|
MedlinePlus related topics: Osteoarthritis
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Uncontrolled, Parallel Assignment, Pharmacokinetics Study
Official Title: A Pharmacokinetic Study of Glucosamine and Chondroitin
Further study details as provided by National Center for Complementary and Alternative Medicine (NCCAM):
Expected Total Enrollment: 70
Study start: April 2004
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.
Eligibility
Ages Eligible for Study: 21 Years and above, Genders Eligible for Study: Both
Accepts Healthy Volunteers
Criteria
Inclusion Criteria:
Exclusion Criteria:
- Allergy to glucosamine, chondroitin, or shellfish
- Liver or kidney disease
- Diabetes mellitus
- Concurrent use of other complementary or alternative therapies
Location and Contact Information
Please refer to this study by ClinicalTrials.gov identifier NCT00086229
Utah
University of Utah Health Sciences Center, Salt Lake City, Utah, 84132, United States; Recruiting
Kalli Cooper 801-581-7724
Christopher G. Jackson, MD, Principal Investigator
More Information
Study ID Numbers: 1-R21-AT001938-01
Last Updated: December 8, 2005
Record first received: June 28, 2004
ClinicalTrials.gov Identifier:
NCT00086229Health Authority: United States: Federal Government