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Clinical Trial Summary

A non-randomized, mono-centric, prospective interventional study that will assess the efficacy of the loco-regional anesthesia PECS on the rate of chronic pain, 6 month after a patient will have either received a mastectomy or a mastectomy associated with axillary nodes dissection, and/or a reconstruction by prosthesis.


Clinical Trial Description

The aim of this study is to assess the care given to treat breast cancer while the patient receives a total mastectomy. It is done by evaluating the technique of anesthesia PECS used during this procedure so that the rate of chronic pain can be measured 6 month after the operation. As well as total mastectomy, patients are also eligible for an axillary lymph node dissection (ALND) and a reconstruction of the breast by prosthesis as options. Other objectives of the study include: - Evaluating the effectiveness of the PECS anesthesia technique on the trajectory of acute post-operative pain and on chronic pain after 12 month of the surgery - Evaluating the type and intensity of the pain - Evaluating the quality of life - Study the link between chronic pain and the trajectory of acute pain. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03023007
Study type Interventional
Source Centre Oscar Lambret
Contact
Status Completed
Phase N/A
Start date April 3, 2017
Completion date August 22, 2019

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