Differences in Extracellular Vesicles From Adipose Tissue of Individuals With Obesity.

NCT06444646 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2025-09-15

No results posted yet for this study

Summary

Our society is characterized by a strong increase in the prevalence of obesity, which often causes the development of cardiovascular and metabolic diseases such as type 2 diabetes. The way(s) obesity is responsible for these diseases, is still insufficiently understood. This study therefore examines the content of human fat tissue storage location- and cell type-specific extracellular vesicles (EVs) in lean and obese individuals, and the possible connection with sex, insulin sensitivity, and the blood-brain barrier.

Conditions

Interventions

OTHER

Adipose tissue biopsy

From each patient, two biopsies will be taken during surgery; one from the subcutaneous and one from the visceral adipose tissue.

OTHER

Blood sampling

From each patient, two venous blood samples (citrate, LiHe and EDTA plasma) will be taken before surgery.

OTHER

Questionnaire

Before bariatric surgery, every patient will fill out questions about general health (physical activity, sedentary behavior, sleeping pattern, ...), physical condition before surgery (nausea, food intake, ...), etc.

OTHER

Patient phenotyping

Length and weight will be measured to calculate body mass index (BMI). Waist and hip circumference will be assessed, as well as blood pressure (both systolic and diastolic) and heart rate at rest. Body composition will be determined using a bioelectrical impedance analysis (BIA) in the hospital. Medication use and comorbidities (that are allowed within the in-/exclusion criteria) will also be derived from the patient's medical files with patient's permission.

Sponsors & Collaborators

  • Research Foundation Flanders

    collaborator OTHER
  • Ziekenhuis Oost-Limburg

    collaborator OTHER
  • Hasselt University

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-02-20
Primary Completion
2026-09-30
Completion
2026-09-30

Countries

  • Belgium

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06444646 on ClinicalTrials.gov