- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00443092
Efficacy of Proprietary Cherry Juice Blend in Osteoarthritis of the Knee
A Double Blind Cross-over Study of the Efficacy of a Proprietary Cherry Juice Blend in Osteoarthritis of the Knee.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The primary objective is to determine if the proprietary tart cherry juice blend improves the pain and function in persons with knee osteoarthritis. A secondary objective is to ascertain if the blend lowers serum uric acid.
This is a prospective double blind, placebo controlled cross-over study.
The study will be performed in the Philadelphia VA Medical Center 1 South Rheumatology Clinic with patients meeting ACR criteria for Kellgren grade 2-3 knee osteoarthritis and 4-9 pain severity on a VAS. Fifty patients will be studied with each having 5 visits. Subjects will take either the proprietary cherry blend or placebo for 6 weeks and then switch. WOMAC pain and function will be the primary outcome with acetaminophen use, walking time and serum uric acid as secondary outcomes.
Study Type
Enrollment (Actual)
Phase
- Phase 4
Contacts and Locations
Study Locations
-
-
Pennsylvania
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Philadelphia, Pennsylvania, United States, 19104
- VA Medical Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Subject is capable of giving informed consent.
- Subject is over 18 years and less than 80 years
Subject has mild to moderate osteoarthritis of the knee based on all of the following 3:
- Meets clinical ACR criteria
- Kellgren score of 2-3 on a Standing Knee x-ray within previous 24 months
- VAS pain score of 4-9 at screening visit
Exclusion Criteria:
- Rheumatoid arthritis or other systemic inflammatory condition
- Chronic pain syndrome (fibromyalgia)
- Corticosteroid medication in last 2 months, either intra-articular or oral
- Intra-articular injections of hyaluronic acid in last 9 months
- Pregnant women (weight gain might confound degree of knee pain)
- Diabetes
- Inability to discontinue prescription medication for arthritis
- Unstable medical conditions that would likely prevent the subject from completing the study
- Food allergies - cherries, apples
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 1
proprietary tart cherry juice blend (8 oz., BID)
|
2 bottles per day for 6 weeks, 1 in the morning and 1 in the evening
|
|
Placebo Comparator: 2
control juice (color matched kool aid blend),(8 oz., BID)
|
2 bottles per day for 6 weeks, 1 in the morning and 1 in the evening
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Improvement in Western Ontario McMaster Osteoarthritis Index (WOMAC) Scores to be taken at Visits 2-5.
Time Frame: Visit 3 (week 6-7), Visit 5 (week 13-14)
|
Visit 3 (week 6-7), Visit 5 (week 13-14)
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Determine if there is a decrease in amount of non-prescription pain medication taken and/or improvement in score on a timed walking test (Visits 2,3,4,5).
Time Frame: Visit 3 (week 6-7), Visit 5 (week 13-14)
|
Visit 3 (week 6-7), Visit 5 (week 13-14)
|
|
Determine if there is a decrease in serum uric acid levels. (Visits 1,3,5)
Time Frame: Visit 3 (week 6-7), Visit 5 (week 13-14)
|
Visit 3 (week 6-7), Visit 5 (week 13-14)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: H. R Schumacher, M.D., VA Medical Center, Philadelphia & University of Pennsylvania
Publications and helpful links
General Publications
- Altman R, Asch E, Bloch D, Bole G, Borenstein D, Brandt K, Christy W, Cooke TD, Greenwald R, Hochberg M, et al. Development of criteria for the classification and reporting of osteoarthritis. Classification of osteoarthritis of the knee. Diagnostic and Therapeutic Criteria Committee of the American Rheumatism Association. Arthritis Rheum. 1986 Aug;29(8):1039-49. doi: 10.1002/art.1780290816.
- Jacob RA, Spinozzi GM, Simon VA, Kelley DS, Prior RL, Hess-Pierce B, Kader AA. Consumption of cherries lowers plasma urate in healthy women. J Nutr. 2003 Jun;133(6):1826-9. doi: 10.1093/jn/133.6.1826.
- Pincus T, Koch G, Lei H, Mangal B, Sokka T, Moskowitz R, Wolfe F, Gibofsky A, Simon L, Zlotnick S, Fort JG. Patient Preference for Placebo, Acetaminophen (paracetamol) or Celecoxib Efficacy Studies (PACES): two randomised, double blind, placebo controlled, crossover clinical trials in patients with knee or hip osteoarthritis. Ann Rheum Dis. 2004 Aug;63(8):931-9. doi: 10.1136/ard.2003.020313. Epub 2004 Apr 13.
- BLAU LW. Cherry diet control for gout and arthritis. Tex Rep Biol Med. 1950;8(3):309-11. No abstract available.
- Connolly DA, McHugh MP, Padilla-Zakour OI, Carlson L, Sayers SP. Efficacy of a tart cherry juice blend in preventing the symptoms of muscle damage. Br J Sports Med. 2006 Aug;40(8):679-83; discussion 683. doi: 10.1136/bjsm.2005.025429. Epub 2006 Jun 21.
- Seeram NP, Momin RA, Nair MG, Bourquin LD. Cyclooxygenase inhibitory and antioxidant cyanidin glycosides in cherries and berries. Phytomedicine. 2001 Sep;8(5):362-9. doi: 10.1078/0944-7113-00053.
- He YH, Zhou J, Wang YS, Xiao C, Tong Y, Tang JC, Chan AS, Lu AP. Anti-inflammatory and anti-oxidative effects of cherries on Freund's adjuvant-induced arthritis in rats. Scand J Rheumatol. 2006 Sep-Oct;35(5):356-8. doi: 10.1080/03009740600704155.
- Johanson NA, Liang MH, Daltroy L, Rudicel S, Richmond J. American Academy of Orthopaedic Surgeons lower limb outcomes assessment instruments. Reliability, validity, and sensitivity to change. J Bone Joint Surg Am. 2004 May;86(5):902-9. doi: 10.2106/00004623-200405000-00003.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CP100M
- VA MIRB ID # 00981
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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