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Multiomic Evaluation of the Effect of Artichoke By-products Supplementation Rich in Hydroxycinnamic Acids, Integrated Into an Energy-restricted Mediterranean Diet, on the Prevention of Type 2 Diabetes.

Status: Recruiting
Location: See location...
Intervention Type: Behavioral, Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The ARTI-UP study evaluates whether daily consumption of a supplement made from artichoke by-products, rich in hydroxycinnamic acids (HCAs), in combination with an energy-restricted Mediterranean diet (erMeDiet), can improve glycaemic control, reduce insulin resistance and contribute to weight loss in subjects with overweight or obesity. In addition, it seeks to understand the biological mechanisms involved using omic techniques and to establish predictive biomarkers that will enable progress towards personalised nutrition strategies.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: t
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• BMI between 25.0 and 35.0 kg/m²

• HOMA-IR ≥ 2.5.

• Adequate physical examination and vital signs or clinically irrelevant to the intervention (those not related to metabolic health).

• Subjects must be able to understand and be willing to sign the informed consent form, and must comply with all study procedures and requirements.

• Subjects must have a stable means of communication, either by email and/or telephone.

Locations
Other Locations
Spain
University of Navarra
RECRUITING
Pamplona
Contact Information
Primary
Idoia Ibero, PhD
iibero@unav.es
+34 948 425 744
Time Frame
Start Date: 2026-02
Estimated Completion Date: 2027-12
Participants
Target number of participants: 150
Treatments
Experimental: Intervention group: erMeDiet + artichoke capsules
Participants will follow a energy-restricted Mediterranean diet and consume artichoke by-product capsules daily for 16 weeks.
Placebo_comparator: Control group: erMeDiet + placebo capsules
Participants will follow an energy-restricted Mediterranean diet and consume placebo capsules daily for 16 weeks.
Related Therapeutic Areas
Sponsors
Collaborators: Hospital of Navarra, University of Navarra
Leads: Clinica Universidad de Navarra, Universidad de Navarra

This content was sourced from clinicaltrials.gov

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