Expired Study
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New York, New York 10065


Purpose:

The goal of the study is measure breast sensations after breast surgery. The results of this study will help surgeons better understand breast sensations and may improve the way surgery is done.


Criteria:

Inclusion Criteria: - The Samples used will be derived from three cohorts below and will only include patients who have completed mastectomy or reconstruction within 1-5 years of enrollment. - Patients who have undergone immediate, two-stage expander/implant postmastectomy reconstruction - Patients who have undergone immediate, autogenous tissue flap reconstruction following mastectomy - Patients who have undergone mastectomy alone - Patients at least 21 years of age - Patients who completed mastectomy ± immediate post-mastectomy reconstruction at least one year but no longer than five years prior to study entry Exclusion Criteria: - Patients who have had any of the following: - delayed reconstruction (no reconstruction at time of surgery) combined autogenous tissue/implant breast reconstruction, and/or - Patients who have a pre-surgical history of complex regional pain syndrome - Patients who have had radiation therapy - Patients who have had a local recurrence - Patients who do not speak the English language (validated translations of key questionnaires are not available).


NCT ID:

NCT00625924


Primary Contact:

Principal Investigator
Andrea Pusic, MD
Memorial Sloan-Kettering Cancer Center


Backup Contact:

N/A


Location Contact:

New York, New York 10065
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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