Acupuncture to Reduce Chemotherapy-induced Peripheral Neuropathy Severity During Neoadjuvant or Adjuvant Weekly Paclitaxel Chemotherapy in Breast Cancer Patients
| Status: | Active, not recruiting |
|---|---|
| Conditions: | Breast Cancer, Cancer, Neurology |
| Therapuetic Areas: | Neurology, Oncology |
| Healthy: | No |
| Age Range: | 21 - Any |
| Updated: | 3/6/2019 |
| Start Date: | February 2015 |
| End Date: | February 2020 |
Acupuncture to Reduce Chemotherapy-induced Peripheral Neuropathy Severity During Neoadjuvant or Adjuvant Weekly Paclitaxel Chemotherapy in Breast Cancer Patients: A Pilot Study
The purpose of this study is to find out the effects of acupuncture on reducing nerve damage.
Acupuncture is a medical technique of inserting very thin needles into the "energy points" on
the body with the aim to restore health and well-being. It has been used widely to treat
pain, such as lower back pain and joint pain. In this study the investigators will assess if
acupuncture can be used to ease the pain, tingling and numbness that may be caused by
chemotherapy and improve quality of life during chemotherapy.
Acupuncture is a medical technique of inserting very thin needles into the "energy points" on
the body with the aim to restore health and well-being. It has been used widely to treat
pain, such as lower back pain and joint pain. In this study the investigators will assess if
acupuncture can be used to ease the pain, tingling and numbness that may be caused by
chemotherapy and improve quality of life during chemotherapy.
Inclusion Criteria:
Screening Phase:
- Age 21 or older.
- Histologically proven stage I-III carcinoma of the breast.
- Plan to receive adjuvant or neoadjuvant chemotherapy that includes weekly paclitaxel.
- Eastern Cooperative Oncology Group performance status 0-2 (see Appendix B).
- The patient is aware of the nature of his/her diagnosis, understands the study
regimen, its requirements, risks, and discomforts, and is able and willing to sign an
informed consent form.
- Proficiency in English with the ability to speak and read English.
Exclusion Criteria:
- Known metastatic (stage IV) breast cancer involvement.
- Pre-existing peripheral neuropathy within 28 days of screening consent
- Currently taking anti-neuropathy medication such as gabapentin, pregabalin,
duloxetine, or glutamine.
Intervention Phase:
- Age 21 or older.
- Histologically proven stage I-III carcinoma of the breast.
- Receiving adjuvant or neoadjuvant chemotherapy that includes a taxane.
- Eastern Cooperative Oncology Group performance status 0-2
- The patient is aware of the nature of his/her diagnosis, understands the study
regimen, its requirements, risks, and discomforts, and is able and willing to sign an
informed consent form.
- Proficiency in English with the ability to speak and read English
- While on neurotoxic chemotherapy, has developed NCI-CTC grade 2 CIPN
Exclusion Criteria:
- Known metastatic (stage IV) breast cancer involvement.
- Pre-existing peripheral neuropathy within 28 days of screening consent.
- Currently taking anti-neuropathy medication such as gabapentin, pregabalin,
duloxetine, or glutamine.
We found this trial at
2
sites
Click here to add this to my saved trials
1275 York Ave
New York, New York 10021
New York, New York 10021
(212) 639-2000
Phone: 646-888-4941
Memorial Sloan Kettering Cancer Center Memorial Sloan Kettering Cancer Center — the world's oldest and...
Click here to add this to my saved trials