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RECRUITING
NCT06907810
NA

Study of Lipid Mediators in Chronic Postoperative Pain - LICP

Sponsor: Université Catholique de Louvain

View on ClinicalTrials.gov

Summary

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.

Official title: Study of Lipid Mediators in Chronic Postoperative Pain Following Breast Cancer Surgery

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

300

Start Date

2025-03-12

Completion Date

2027-03-31

Last Updated

2025-04-02

Healthy Volunteers

No

Interventions

OTHER

Blood sample + questionnaire

* blood sample before tumor surgery and at every follow-up visit * questionnaire before tumor surgery and at every follow-up visit

Locations (1)

Cliniques universitaires Saint-Luc (UCLouvain)

Brussels, Brussels Capital, Belgium