Study to Assess Breast Sensation Before and After Breast Cancer Treatment

Withdrawn before enrolling · Not applicable

Conditions studied: Breast Reconstruction, Ductal Carcinoma In-situ

In brief

The purpose of this study is to establish techniques for evaluating breast cutaneous sensation at baseline and following either lumpectomy or mastectomy for breast cancer.

Key facts

Study ID

NCT02817607

Run by

Duke University

People needed

0

Starts

2016-12-01

Expected to finish

2018-08-01

Last updated by the study team

2019-05-07

Who can join

Age: 25 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• patients diagnosed with ductal carcinoma in-situ (DCIS) or invasive breast cancer
• patients that have been offered lumpectomy or mastectomy for surgical treatment
• patients with a high risk of breast cancer and are pursuing prophylactic mastectomies

You may not qualify if…

• metastatic malignancy of any kind
• subjects will not have breast surgery as a portion of their breast cancer care
• between 25 and 65 years old
• subjects with breast implants or a history of prior breast implants
• subjects that have had prior breast reduction surgery
• subjects who have had radiation to one of both breasts in the past
• subjects who cannot give informed consent

Where it is running

• Duke University Medical Center — Durham, North Carolina, United States

Full record on ClinicalTrials.gov

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