Actively Recruiting

Phase Not Applicable
Age: 23Years - 65Years
All Genders
NCT07433998

Effect of a Ginger-Based Beverage on Inflammation, Oxidative Stress, and Endothelial Function

Led by Javier Marhuenda · Updated on 2026-03-04

50

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Randomized, double-blind, parallel, placebo-controlled clinical trial designed and conducted to evaluate the effect of daily consumption of ginger, on parameters related to inflammation, oxidative stress, and endothelial damage in adults with excess adiposity.

CONDITIONS

Official Title

Effect of a Ginger-Based Beverage on Inflammation, Oxidative Stress, and Endothelial Function

Who Can Participate

Age: 23Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male and female participants.
  • Age between 23 and 65 years.
  • Body mass index (BMI) > 27.5 kg/m².
  • Absence of diagnosed chronic diseases.
  • Not receiving pharmacological treatment or dietary supplementation on a regular basis.
  • Ability to understand the study procedures and willingness to comply with study requirements.
Not Eligible

You will not qualify if you...

  • Presence of acute or chronic diseases not specified in the inclusion criteria.
  • Ongoing chronic pharmacological treatment or active use of dietary supplements.
  • Major surgery within the previous three months.
  • Current smokers or recent former smokers (less than six months since cessation).
  • History of clinically relevant food allergies or eating disorders.
  • Concurrent participation in another clinical trial or research study.
  • Pregnancy or breastfeeding.
  • Following an active weight-loss diet.
  • Investigator's judgment of unsuitability for study participation.

AI-Screening

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Trial Site Locations

Total: 1 location

1

UCAM

Murcia, Spain

Actively Recruiting

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Research Team

J

Javier Marhuenda Hernández

CONTACT

U

Universidad Católica San Antonio de Murcia

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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