RecruitingNCT07447440

Role of Pro-Resolving Lipid Mediators in Obesity-Associated Diseases

Unraveling the Role of Pro-Resolving Lipid Mediators of Inflammation and Their Receptors in Obesity-Associated Diseases: New Therapeutic Approaches for Maresin 1 (RESOLBE)


Sponsor

Clinica Universidad de Navarra, Universidad de Navarra

Enrollment

60 participants

Start Date

Oct 15, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

The main objective of this project is to determine the possible association between the levels of certain bioactive lipids, which the body produces from dietary fatty acids, and tumor characteristics in breast cancer patients, as well as their relationship with overweight/obesity. Specific objectives are: * To analyse anthropometric and body composition changes. * To evaluate physical activity level. * To determine dietary profile. * To determine the adherence to Mediterranean dietary pattern. * To assess the quality of life. * To determine levels of specialized pro-resolving lipid mediators The target sample size is 60 subjects. Participants will be allocated in four groups: * Group 1: Postmenopausal healthy women with overweight/obesity (n=15) * Group 2: Postmenopausal healthy women with normoweight (n=15) * Group 3: Postmenopausal women with breast cancer and overweight/obesity (n=15) * Group 4: Postmenopausal women with breast cancer and normoweight (n=15)


Eligibility

Sex: FEMALE

Plain Language Summary

Simplified for easier understanding

This study is investigating a class of natural anti-inflammatory molecules called pro-resolving lipid mediators, and whether their levels are different in postmenopausal women with obesity and in those with breast cancer. The goal is to understand how these molecules relate to inflammation in obesity-related diseases. **You may be eligible if (Healthy participants):** - You are postmenopausal (at least 1 year without a period) - You are of normal weight, overweight, or obese - You have no personal history of cancer - Your weight has been stable for the past 3 months **You may be eligible if (Breast cancer participants):** - You are postmenopausal - You have early-stage luminal breast cancer (Stage I or II) requiring surgery without pre-operative treatment **You may NOT be eligible if:** - You have a personal history of cancer (healthy group) - You are currently on a weight loss program, have had bariatric surgery, or are taking diabetes or hormone replacement medications - You have significant gastrointestinal disease, liver disease (other than fatty liver), heavy alcohol use, or psychiatric impairment - Your breast cancer is Stage III or higher Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERObservational study (baseline)

Data will be collected at a single time point.

OTHERObservational study (baseline and 1 year)

Data will be collected at two time points during the study period.


Locations(2)

Center for Nutrition Research

Pamplona, Navarre, Spain

Clínica Universidad de Navarra

Pamplona, Navarre, Spain

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07447440


Related Trials