Phase
Condition
Lactose Intolerance
Mood Disorders
Vomiting
Treatment
Acupuncture
Aromatherapy
Clinical Study ID
Ages > 18 Female
Study Summary
Eligibility Criteria
Inclusion
i) Inclusion
At least 18 years of age on the day of signing informed consent
Patient has a diagnosis of breast cancer
Patient is planned to start Adriamycin and Cytoxan chemotherapy
ii) Exclusion
Patients who are unable to adhere to the protocol or treatment schedule
Patients who have a concurrent illness or take medication that induces nausea independent of chemotherapy
Patients undergoing radiotherapy or hormone therapy during chemotherapy treatments
Patients who have a sensitive and/or poor sense of smell
Patients who are allergic to essential oils, specifically peppermint, ginger, and/or lavender
Patients who are already using essential oils or acupuncture for symptom management and are unwilling to stop while participating in this study
Patients who are afraid of or unwilling to receive acupuncture stimulation
Patients who are allergic to stainless steel needles
Thrombocytopenia (Platelets < 20,000)
Patients who have received aromatherapy and/or acupuncture treatment within 1 week of starting treatment on this study
Study Design
Connect with a study center
Englewood Health
Englewood, New Jersey 07631
United StatesSite Not Available
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