Sensory Morbidity Following Breast Surgery

Completed

Conditions studied: Breast Cancer

In brief

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.

Key facts

Study ID

NCT00625924

Run by

Memorial Sloan Kettering Cancer Center

People needed

290

Starts

2008-02-01

Expected to finish

2014-01-01

Last updated by the study team

2014-01-16

Who can join

Age: 21 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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).

Where it is running

• Memorial Sloan Kettering Cancer Center — New York, New York, United States

Full record on ClinicalTrials.gov

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