Heavy Metal Exposure in Predicting Peripheral Neuropathy in Patients With Stage I-III Breast Cancer Undergoing Chemotherapy
Completed
Conditions studied: Male Breast Cancer, Neurotoxicity, Peripheral Neuropathy, Stage IA Breast Cancer, Stage IB Breast Cancer, Stage II Breast Cancer, Stage IIIA Breast Cancer, Stage IIIB Breast Cancer, Stage IIIC Breast Cancer
In brief
This research trial studies heavy metal exposure in predicting peripheral neuropathy in patients with stage I-III breast cancer undergoing chemotherapy. Studying samples of blood and urine in the laboratory for heavy metal exposure from patients receiving chemotherapy may help doctors find out whether side effects from chemotherapy are related to heavy metal exposure.
Key facts
- Study ID
- NCT01982591
- Run by
- Fox Chase Cancer Center
- People needed
- 115
- Starts
- 2011-01-03
- Expected to finish
- 2015-03-24
- Last updated by the study team
- 2017-06-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients must have histologically confirmed invasive mammary carcinoma; any histologic sub-type allowed
- Patients must be diagnosed with stage I, II or III breast cancer
- Patients must be undergoing treatment with an adjuvant or neoadjuvant cytotoxic chemotherapy that includes a taxane, specifically paclitaxel, nab-paclitaxel (Abraxane), or docetaxel
- Patients may have received prior endocrine and/or radiation therapy
- Patients must have the ability to understand and the willingness to sign a written informed consent document
You may not qualify if…
- Patients who have been previously treated with cytotoxic chemotherapy
- Patients with pre-existing peripheral neuropathy
Where it is running
- Paoli Memorial Hospital — Paoli, Pennsylvania, United States
- Fox Chase Cancer Center — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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