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Study of Lipid Mediators in Chronic Postoperative Pain - LICP

NCT06907810·1 site·ClinicalTrials.gov

What this study is about

Take this into the appointment.

Saves the questions and what to expect into your notes, next to the visit they belong to.

Keep this study

Martine Berlière, MD, PhD
CONTACT
00327641075 martine.berliere@saintluc.uclouvain.be
Lisa Martin, MSC
CONTACT
lisa.martin@uclouvain.be

Lead

Université Catholique de Louvain

With

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Age

18–any

Sex

FEMALE

Healthy volunteers

Not accepted

You may be eligible if

Women older than 18 years
Newly diagnosed primary invasive or non-invasive breast cancer, requiring surgical excision of the tumor, with or without axillary surgery
Able to give informed consent

You may not be if

Men
Women aged less than 18 years
Pregnant women
History of major psychiatric disorders
Previous breast or axillary surgery, recurrent disease or detectable metastatic disease at the time of diagnosis
Unable to give informed consent

The record

StatusRecruiting

PhaseNo phase

Taking part300

StartedMar 2025

UpdatedApr 2, 2025

Conditions

Breast Cancer Female Postoperative Pain

Where1

Cliniques universitaires Saint-Luc (UCLouvain)
Brussels, Brussels Capital, Belgium

Clareo Health | Study of Lipid Mediators in Chronic Postoperative Pain - LICP