Efficacy of Proprietary Cherry Juice Blend in Osteoarthritis of the Knee

Sponsor
CherryPharm (Industry)
Overall Status
Completed
CT.gov ID
NCT00443092
Collaborator
(none)
59
1
2
45
1.3

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: proprietary cherry juice blend (food)
  • Other: control juice (kool aid blend)
Phase 4

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 Design

Study Type:
Interventional
Actual Enrollment :
59 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
A Double Blind Cross-over Study of the Efficacy of a Proprietary Cherry Juice Blend in Osteoarthritis of the Knee.
Study Start Date :
Mar 1, 2007
Actual Primary Completion Date :
Jun 1, 2010
Actual Study Completion Date :
Dec 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Experimental: 1

proprietary tart cherry juice blend (8 oz., BID)

Other: proprietary cherry juice blend (food)
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)

Other: control juice (kool aid blend)
2 bottles per day for 6 weeks, 1 in the morning and 1 in the evening

Outcome Measures

Primary Outcome Measures

  1. 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 Outcome Measures

  1. 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)]

  2. 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)]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 VA Medical Center Philadelphia Pennsylvania United States 19104

Sponsors and Collaborators

  • CherryPharm

Investigators

  • Principal Investigator: H. R Schumacher, M.D., VA Medical Center, Philadelphia & University of Pennsylvania

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00443092
Other Study ID Numbers:
  • CP100M
  • VA MIRB ID # 00981
First Posted:
Mar 5, 2007
Last Update Posted:
Aug 3, 2012
Last Verified:
Aug 1, 2012

Study Results

No Results Posted as of Aug 3, 2012