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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.

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00443092
Enrollment
59
Registered
2007-03-05
Start date
2007-03-31
Completion date
2010-12-31
Last updated
2012-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis

Keywords

osteoarthritis, gout, pain, uric acid, tart cherry, alternative medicine, knees

Brief summary

The primary purpose of this research study is to test the ability of a proprietary cherry juice blend to be helpful in the treatment of osteoarthritis (OA) of the knee.

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.

Interventions

OTHERproprietary cherry juice blend (food)

2 bottles per day for 6 weeks, 1 in the morning and 1 in the evening

OTHERcontrol juice (kool aid blend)

2 bottles per day for 6 weeks, 1 in the morning and 1 in the evening

Sponsors

CherryPharm
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

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: 1. Meets clinical ACR criteria 2. Kellgren score of 2-3 on a Standing Knee x-ray within previous 24 months 3. 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

Design outcomes

Primary

MeasureTime frame
Improvement in Western Ontario McMaster Osteoarthritis Index (WOMAC) Scores to be taken at Visits 2-5.Visit 3 (week 6-7), Visit 5 (week 13-14)

Secondary

MeasureTime 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).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)Visit 3 (week 6-7), Visit 5 (week 13-14)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026