Study of Lipid Mediators in Chronic Postoperative Pain - LICP
Recruiting
N/A
Interventional Study
Breast Cancer Female
Postoperative Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Screening
- Participants needed
- 300 (estimated)
- Sponsor
- Université Catholique de Louvain · Other
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About This Trial
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 …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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
Exclusion Criteria:
* Men
* Women aged less than 18 years
* Pregnant women
*…
Contacts