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Clinical Trials/NCT06163937
NCT06163937
Completed
Not Applicable

Examining the Acute Effects of Two Different Fruit Juices (Orange Juice and Mixed Fruit Juice Consisted of Apple, Orange, Grape, and Pomegranate) on Postprandial Glycemic Responses and Satiety in Healthy Individuals

Agricultural University of Athens1 site in 1 country10 target enrollmentStarted: September 1, 2023Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
10
Locations
1
Primary Endpoint
Capillary blood glucose responses

Overview

Brief Summary

This study investigated the acute effects of two fruit juices on postprandial glycemic responses and satiety in healthy individuals

Detailed Description

This study aimed to 1. Determine the glycemic index and glycemic load of two types of fruit juices (orange juice and mixed fruit juice consisted of apple, orange, grape, and pomegranate) and 2. Investigate the effects of these two fruit juices on postprandial glycemic responses and satiety in healthy individuals

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Other
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Masking Description

Triple-blind

Eligibility Criteria

Ages
18 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • non-smoking
  • non-diabetic and normotensive men and women
  • body mass index between 18.5 and 25 kg/m2

Exclusion Criteria

  • severe chronic disease (e.g. cardiovascular diseases, diabetes mellitus, kidney or liver conditions, endocrine conditions)
  • gastrointestinal disorders
  • pregnancy
  • lactation
  • competitive sports
  • alcohol abuse
  • drug dependency

Outcomes

Primary Outcomes

Capillary blood glucose responses

Time Frame: 2 hours

Clinically useful change in blood glucose, defined as the restoration of glucose within normal limits during the 2hr glucose tolerance test

Glycemic index

Time Frame: 2 hours

Glucose solution (50 g) was the reference food (GI = 100%) against which all test foods were compared. Subjects arrived at the laboratory at eight to nine o'clock in the morning after 10-12 h overnight fast. Each subject was fed equivalent 50 g available carbohydrate of test foods or reference food in random order. To minimize day to day variation of glucose tolerance, the reference food was tested in triplicate in each subject. All test and reference foods were served with 250 mL of water. An automatic lancet device and glucometer (calibrated MediSmart Ruby glucose meter with a lancing device, Lilly-PHARMASERV SA, Greece) was used for finger capillary blood samples. Blood samples were taken immediately before the start of the study (0 min) and 15, 30, 45, 60, 90 and 120 min after the start of eating.

Secondary Outcomes

  • Blood pressure(2 hours)
  • Subjective appetite ratings(2 hours)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Aimilia Papakonstantinou

Assistant Professor

Agricultural University of Athens

Study Sites (1)

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