Actively Recruiting
Effect of a Nutritional Product Containing Carob Extract on Carbohydrate Metabolism in Glucose-intolerant Subjects
Led by Universidad Católica San Antonio de Murcia · Updated on 2026-02-19
30
Participants Needed
1
Research Sites
22 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Randomized, controlled, double-blind clinical trial with two parallel arms based on the product consumed (experimental product and placebo product) and conducted at a single center, to measure the efficacy of the liquid NUTIFOOD product (nutritional product with carob extract) on carbohydrate metabolism.
CONDITIONS
Official Title
Effect of a Nutritional Product Containing Carob Extract on Carbohydrate Metabolism in Glucose-intolerant Subjects
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Subjects of both sexes aged 18-65 years.
- Diagnosis of glucose intolerance according to the American Diabetes Association criteria, including impaired fasting glucose (100-125 mg/dl), impaired glucose tolerance (2-hour plasma glucose 140-199 mg/dl), or glycated hemoglobin between 5.7% and 6.4%.
- Body mass index between 20-35 kg/m².
- Stable dietary habits with no weight gain or loss greater than 5 kg in the last ten weeks.
- Ability to understand the study and willingness to comply with study procedures and requirements.
You will not qualify if you...
- Use of medications that may interfere with glucose metabolism.
- History of any type of liver or kidney disease.
- Alcohol consumption greater than 20 g/day.
- History of allergic hypersensitivity or poor tolerance to any component of the study products.
- Participation in another clinical trial within the three months prior to the study.
- Lack of willingness or inability to comply with clinical trial procedures.
- Pregnant or breastfeeding women.
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
UCAM HiTech, Sport & Health Innovation Hub
Murcia, Spain
Actively Recruiting
Research Team
F
Francisco Javier López Román
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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