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Study identifier: NCT06123286 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Tart Cherry and Omega-3's for Aromatase Inhibitor Musculoskeletal Symptoms

Condition: Breast Cancer · Aromatase Inhibitor Associated Musculoskeletal Symptoms (AIMSS) · Joint Pain  ·  Sponsor: Philip Chang

PhaseEARLY_Phase 1
Planned participants30
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Both Tart Cherry and Omega 3 FAs have better side effect profiles compared to other commonly used medications for AIMSS, such as nonsteroidal anti-inflammatories, steroids, and serotonin norepinephrine reuptake inhibitors. Additionally, in our clinics we often find that patients tend to be more receptive to taking a supplement as opposed to an additional medication. Further, both Tart Cherry concentrate and fish oil have beneficial properties for helping with joint stiffness in general, in addition to other health issues like insomnia. There is preliminary evidence in mouse models that when given together, these supplements may have an even greater anti-inflammatory effect than when taken separately14. Although to our knowledge, no human studies have tested this hypothesis. This study has been designed to test the hypothesis that Tart Cherry and fish oil when given in combination over a 12-week period could produce beneficial changes in joint function when compared to Tart Cherry or fish oil in isolation in an obese breast cancer population experiencing AIMSS. Secondary outcomes to be assessed include pain, functional performance, quality of life and cognition.

This description comes directly from the study's public registry record.

Talk to the study team

Clinical Trial Navigator  ·  3104232133  ·  GroupCancerTrialInformation@cshs.org

Always discuss trial participation with your own doctor first.

Locations (2)

Cedars-Sinai Medical CenterLos Angeles, California, United StatesRecruiting
CS Cancer at the Hunt Cancer CenterTorrance, California, United StatesNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT06123286