Breast Cancer Clinical Trial
Acupuncture and Gabapentin for Hot Flashes Among Breast Cancer Survivors
Summary
Overall Objectives: The overarching goal is to compare the effectiveness of acupuncture and gabapentin to their respective placebo controls in the treatment of hot flashes in breast cancer patients. The investigators primary specific aim will focus on determining the magnitude of response to placebo acupuncture versus placebo pills on hot flashes (HFs).
Eligibility Criteria
Inclusion Criteria:
Women 18 years or older with a history of Stage I, II or III breast cancer for at least 12 months.
Have been seen by an oncologist within the previous 6-month period and determined to be free of disease by clinical examination and history;
Experienced at least two hot flashes daily over the seven-day screening period as based on the Daily Hot Flash Diary.
Hot flashes have been present for at least a month before study entry.
Willing to use non-hormonal contraceptives during the duration of the study if patient is premenopausal.
Exclusion Criteria:
Having metastatic breast cancer ( IV)
Currently on chemotherapy or radiation therapy as adjuvant treatment
Started hormonal therapies such as tamoxifen or aromatase inhibitors within the last 4 weeks; or plan to change or terminate hormonal therapies in the next 14 weeks.
Started or changed with treatments for hot flashes, such as SSRIs or clonidine within the last 4 weeks; or plan to change or terminate these therapies in the next 14 weeks.
Current use of estrogen and/or progestin.
Pregnancy
Breast feeding
Bleeding disorder or current use of warfarin or heparin by patient history because of the use of needles.
Previous use of gabapentin for hot flashes.
Current use of any anti-convulsant.
Renal dysfunction defined as serum creatinine concentration above 1.25 times the upper limit of normal
Known allergy to gabapentin.
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There is 1 Location for this study
Philadelphia Pennsylvania, 19104, United States
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