Breast Cancer Clinical Trial

Sensory Morbidity Following Breast Surgery

Summary

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.

View Eligibility Criteria

Eligibility 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).

Study is for people with:

Breast Cancer

Estimated Enrollment:

290

Study ID:

NCT00625924

Recruitment Status:

Completed

Sponsor:

Memorial Sloan Kettering Cancer Center

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There is 1 Location for this study

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Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States

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Study is for people with:

Breast Cancer

Estimated Enrollment:

290

Study ID:

NCT00625924

Recruitment Status:

Completed

Sponsor:


Memorial Sloan Kettering Cancer Center

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