Effect of the Imera Cultivar Carob in Postprandial Glycemia

NCT ID: NCT06906965

Last Updated: 2025-04-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-01-31

Study Completion Date

2024-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

An acute randomized crossover study on the effect of a carob beverage on postprandial glycemic response

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

This is an acute randomized crossover study on the effect of an Imera cultivar carob beverage on postprandial glycemic response in healthy individuals as opposed to sucrose-based beverage containing sugar in alike concentration

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Postprandial Glucose Regulation

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Carob beverage

The participants consumed a carob beverage prepared with 30 g of Imera cultivar carob powder dissolved in water

Group Type EXPERIMENTAL

Carob beverage

Intervention Type OTHER

The participants consumed a carob beverage made with 30gr of Imera carob cultivar powder in water

Sucrose beverage

The participants consumed a sucrose beverage made containing 14 g of sugar, matched to the sugar concentration of the experimental beverage

Group Type ACTIVE_COMPARATOR

Sucrose beverage

Intervention Type OTHER

The participants consumed a sucrose beverage made with 14gr of sugar in alike concentration with sugars in the experimental beverage

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Carob beverage

The participants consumed a carob beverage made with 30gr of Imera carob cultivar powder in water

Intervention Type OTHER

Sucrose beverage

The participants consumed a sucrose beverage made with 14gr of sugar in alike concentration with sugars in the experimental beverage

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* healthy male adults of normal body fat mass

Exclusion Criteria

* obesity (according to body fat mass), type 1 Diabetes, hypertension and other cardiovascular diseases, thyroid disorder, liver, kidney, gastrointestinal disease, mental illness, use of nutraceutical supplements or natural products for weight loss and the background of dietitian/nutritionist.
Minimum Eligible Age

18 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Harokopio University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Andriana C. Kaliora

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Department of Nutrition and Dietetics, HarokopioUniversity of Athens

Kallithea, Attica, Greece

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Greece

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

016713

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

CAROB_GLUCOSE_147

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Postprandial Response to Fruit Juice
NCT07103083 RECRUITING NA