Clinical Trials Directory

Trials / Terminated

TerminatedNCT00892268

Acupuncture or Medication in Reducing Pain in Postmenopausal Women With Breast Cancer and Joint Pain

Acupuncture for the Treatment of Aromatase Inhibitor Associated Joint Pain in Post-Menopausal Breast Cancer Patients

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
68 (estimated)
Sponsor
University of Arizona · Academic / Other
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

RATIONALE: Acupuncture may reduce joint pain in postmenopausal women with breast cancer. It is not yet known whether acupuncture is more effective than standard therapy analgesics in decreasing joint pain caused by aromatase inhibitors. PURPOSE: This randomized phase II trial is studying acupuncture to see how well it works compared with medication in reducing pain in postmenopausal women with breast cancer and joint pain.

Detailed description

OBJECTIVES: Primary * To evaluate the efficacy of acupuncture in reducing pain, defined by improvements in overall WOMAC score at 6 weeks, in post-menopausal women with breast cancer and aromatase inhibitor (AI)-associated arthralgia. Secondary * To identify biologic correlates to acupuncture efficacy in this specific syndrome of AI-associated pain. * To evaluate the efficacy of acupuncture in these patients. OUTLINE: Patients are randomized to 1 of 2 treatment arms: * Arm I: Patients undergo acupuncture for 20-30 minutes, on the appropriate pain points on the anterior portion of the body alternating with posterior portion of the body, thrice weekly for 2 weeks and then twice weekly for 3 weeks. * Arm II: Patients receive standard-of-care analgesics (i.e., NSAIDs, narcotics, acetaminophen, or other) for 5 weeks. Patients not responding to analgesia may cross over to arm I. Patients are assessed periodically for improvement in pain, menopausal symptoms, and overall quality of life by the WOMAC, Brief Pain Inventory, and FACT-ES questionnaires. Blood samples are collected at baseline, 6 weeks, 3 months, and 6 months for biomarker studies of brain-derived neurotrophic factor and serotonin-transporter gene polymorphisms levels by ELISA. After completion of study therapy, patients are followed at 1 week, 6 weeks, 3 months, and 6 months.

Conditions

Interventions

TypeNameDescription
PROCEDUREacupuncture therapyUndergo acupuncture
PROCEDUREpain therapyReceive standard care

Timeline

Start date
2008-01-01
Primary completion
2009-10-01
Completion
2009-10-01
First posted
2009-05-04
Last updated
2010-04-27

Source: ClinicalTrials.gov record NCT00892268. Inclusion in this directory is not an endorsement.