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| Name | Class |
|---|---|
| Cliniques universitaires Saint-Luc- Université Catholique de Louvain | OTHER |
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This interventional prospective study aims firstly to investigate variations in lipid levels in blood samples and their potential relationship with the duration and/or intensity of post-operative pain. Secondly, it aims to investigate the activation of peripheral blood mononuclear cells and neutrophils in patient blood samples. The study will enrol women aged 18 years or older who have been newly diagnosed with primary invasive or non-invasive breast cancer requiring surgical removal of the tumour, with or without axillary surgery.
The main objectives of the study are To assess whether there is an association between circulating levels of lipid mediators and chronicity (> 3 months) of postoperative pain after breast cancer surgery.
To assess whether circulating levels of lipid mediators can predict chronicity of postoperative pain in breast cancer surgery.
To assess the existence of an association between resected tissue levels of lipid mediators and chronicity of postoperative pain in breast cancer surgery.
To assess whether tissue levels of lipid mediators can predict chronicity of postoperative pain in breast cancer surgery.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Chronic pain | Experimental |
| |
| No chronic pain | Active Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Blood sample + questionnaire | Other |
|
|
| Measure | Description | Time Frame |
|---|---|---|
| Pain intensity | Pain intensity will be evaluated using a standardized questionnaire completed by participants at each medical consultation. | Throughout the study, an average of 2 years |
| Pain duration | Pain duration will be evaluated using a standardized questionnaire completed by participants at each medical consultation. | Throughout the study, an average of 2 years |
| Lipid Mediator Levels in Blood | Lipid mediator levels will be quantified in blood samples by LC-MS methods | Throughout the study, an average of 2 years |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Martine Berlière, MD, PhD | Contact | 00327641075 | martine.berliere@saintluc.uclouvain.be | |
| Lisa Martin, MSC | Contact | lisa.martin@uclouvain.be |
| Name | Affiliation | Role |
|---|---|---|
| Mireille Alhouayek, PhD | Université Catholique de Louvain | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Cliniques universitaires Saint-Luc (UCLouvain) | Recruiting | Brussels | Brussels Capital | 1200 | Belgium |
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| ID | Term |
|---|---|
| D010149 | Pain, Postoperative |
| ID | Term |
|---|---|
| D011183 | Postoperative Complications |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D010146 | Pain |
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| ID | Term |
|---|---|
| D001800 | Blood Specimen Collection |
| D011795 | Surveys and Questionnaires |
| ID | Term |
|---|---|
| D013048 | Specimen Handling |
| D019411 | Clinical Laboratory Techniques |
| D019937 | Diagnostic Techniques and Procedures |
| D003933 | Diagnosis |
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| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D011677 | Punctures |
| D013514 | Surgical Procedures, Operative |
| D008919 | Investigative Techniques |
| D003625 | Data Collection |
| D004812 | Epidemiologic Methods |
| D017531 | Health Care Evaluation Mechanisms |
| D011787 | Quality of Health Care |
| D017530 | Health Care Quality, Access, and Evaluation |
| D011634 | Public Health |
| D004778 | Environment and Public Health |