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Clinical Trials/NCT00443092
NCT00443092
Completed
Phase 4

A Double Blind Cross-over Study of the Efficacy of a Proprietary Cherry Juice Blend in Osteoarthritis of the Knee.

CherryPharm1 site in 1 country59 target enrollmentMarch 2007
ConditionsOsteoarthritis

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Osteoarthritis
Sponsor
CherryPharm
Enrollment
59
Locations
1
Primary Endpoint
Improvement in Western Ontario McMaster Osteoarthritis Index (WOMAC) Scores to be taken at Visits 2-5.
Status
Completed
Last Updated
13 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
March 2007
End Date
December 2010
Last Updated
13 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
CherryPharm

Eligibility Criteria

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)
  • Inability to discontinue prescription medication for arthritis
  • Unstable medical conditions that would likely prevent the subject from completing the study
  • Food allergies - cherries, apples

Outcomes

Primary Outcomes

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)

Secondary Outcomes

  • 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))

Study Sites (1)

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