Expired Study
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San Francisco, California 94143


Purpose:

This trial is part of a larger, longitudinal study of symptoms that occur in the breast surgical scar area and/or ipsilateral arm following breast cancer surgery. Women who develop pain in the breast scar area or ipsilateral arm will be randomized to a placebo patch or a lidocaine patch that they will wear on a daily basis for 12 weeks. We hypothesize that women who wear the lidocaine patch will report a decrease in pain and decreased interference with function compared to women who wear the placebo patch.


Criteria:

Inclusion Criteria: - Adult women >18 years who develop neuropathic pain in the breast scar area and/or ipsilateral arm following breast cancer surgery - Has a healed incision(s) - Has no recurrent disease in the painful area - Is able to read, write and understand English Exclusion Criteria: - Presence of another type of pain that is more severe than the neuropathic pain - Use of an opioid analgesic of greater than 60 mg codeine/day - Is actively trying to become pregnant - Has a medical contraindication to the use of lidocaine - Has an allergy to lidocaine - Is taking a coanalgesic for neuropathic pain.


NCT ID:

NCT00686127


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

San Francisco, California 94143
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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