Actively Recruiting

Phase Not Applicable
Age: 35Years - 36Years
All Genders
Healthy Volunteers
NCT07361887

Deciphering the Effect of Moderate Wine Consumption on Healthy Aging Through Postprandial Extracellular Vesicles.

Led by University of Seville · Updated on 2026-01-23

8

Participants Needed

1

Research Sites

73 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to investigate how moderate wine consumption influences circulating extracellular vesicles (EVs) in healthy adults. EVs are small particles released by cells that carry proteins, lipids, and genetic material, and play important roles in communication between cells. Participants will consume a single serving of red or white wine, and blood samples will be collected before and after consumption to study changes in the composition and function of EVs. The study will also assess how these EVs affect vascular, immune, and brain-related cells. The results are expected to improve our understanding of how moderate wine intake contributes to cardiovascular and brain health.

CONDITIONS

Official Title

Deciphering the Effect of Moderate Wine Consumption on Healthy Aging Through Postprandial Extracellular Vesicles.

Who Can Participate

Age: 35Years - 36Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy adults aged 35 to 65 years
  • Body Mass Index (BMI) between 18.5 and 29.9 kg/m²
  • Non-smokers or ex-smokers for at least 12 months
  • Moderate alcohol consumers (up to 2 units/day for men, up to 1 unit/day for women)
  • Normal fasting glucose and lipid profile at screening
  • Willing and able to avoid alcohol, polyphenol-rich foods, and intense exercise for 48 hours before each visit
  • Able to understand study procedures and provide written informed consent
Not Eligible

You will not qualify if you...

  • History or signs of cardiovascular, liver, kidney, thyroid, gastrointestinal, or metabolic diseases, including diabetes, dyslipidemia, or hypertension
  • Use of medications or supplements affecting glucose, lipid, or inflammatory metabolism
  • Pregnancy or breastfeeding
  • Recent or planned blood donation within the study period
  • Major weight change (>5% body weight) in the last 3 months
  • Participation in another clinical or biomedical study in the past 3 months
  • Known allergy or intolerance to wine, alcohol, or components like sulfites
  • History of alcohol abuse or inability to abstain from alcohol outside the study
  • Unwillingness to receive information about incidental health findings
  • Any condition limiting compliance or increasing study risk, such as psychiatric disorders or inability to follow fasting requirements

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Av. de Sánchez Pizjuán, s/n, 41009 Sevilla Facultad de Medicina . Universidad de Sevilla

Seville, Sevilla, Spain, 41009

Actively Recruiting

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Research Team

S

Sergio Montserrat-de la Paz, Full Professor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

3

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