Viewing Study NCT03023007



Ignite Creation Date: 2024-05-06 @ 9:36 AM
Last Modification Date: 2024-10-26 @ 12:16 PM
Study NCT ID: NCT03023007
Status: COMPLETED
Last Update Posted: 2022-11-21
First Post: 2017-01-10

Brief Title: Study Evaluating the Efficacy of Loco-regional Anaesthesia PECS on Chronic Pain of a Mastectomy
Sponsor: Centre Oscar Lambret
Organization: Centre Oscar Lambret

Study Overview

Official Title: Study Evaluating the Efficacy of Loco-regional Anaesthesia PECS on the Rate of Chronic Pains 6 Month After a Mastectomy Associated or Not With Axillary Node Dissection andor a Reconstruction Prosthesis
Status: COMPLETED
Status Verified Date: 2022-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: PECS
Brief 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 andor a reconstruction by prosthesis
Detailed 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 Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
NIdRCB N2016-A00562-49 OTHER ANSM None