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The Prebiotic Effect of Daily Intake of Orange Juice Affects the Bioavailability of Flavanones?

Influence of the Prebiotic Effect of Orange Juice on the Bioavailability of Flavanones After Chronic Intake of Orange Juice.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03032861
Enrollment
10
Registered
2017-01-26
Start date
2016-09-30
Completion date
2017-02-28
Last updated
2017-04-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intestinal Diseases

Keywords

Orange juice, Microbiota, Prebiotic, Flavanones, Bioavailability

Brief summary

This study aimed investigate the chronic effect of orange juice consumption on gut microbiota and in the bioavailability of flavanones and metabolites by feces, blood and urine analysis.

Detailed description

Non-randomized study with interrupted time series and open-label, in which women were enrolled and advised to not consumed foods containing prebiotic, probiotic and fibers, and citrus fruits and beverages during 30 days before of intervention (n=10; BMI 23.8 kg/m2; 28 years). After 30 days, the participants will consume during 60 days 300 mL of orange juice daily. After 60 days of orange juice intervention, the participants will be submitted to 30 days of washout. Samples of blood, urine and feces will collect in five different occasions (baseline, 30 day, 60 day, 90 day, and 120 day) in order to evaluate the prebiotic effect of orange juice on gut microbiota and in the bioavailability of its flavanones. The recruitment process began in September 2016 and the intervention was carried out from October 2016 to February 2017, and the data analysis will start in February 2017. The sample number took into account variances on blood hesperitin levels with a type I error α = 0.05 and a type II error β = 0.2 (80% power) (Silveira et al., 2015). The minimum sample size should have six individuals into the same group. Considering an approximately 15% dropout rate, the final sample size of study was constituted by 10 women. Primary endpoint is the changes in total bacteria population (Lactobacillus spp., Bifidobacterium spp., and reduction of Clostridium spp.) that can result in increased of butyric, acetic, and propionic acid concentrations, and reduction of ammonium production. Secondary endpoint is enhancement of bioavailability of flavanones (hesperitin, naringenin) and metabolites in the blood, urine and feces. Kolmogorov Smirnov and Levene test will be used to assess the normality and homogeneity of data, respectively. One-way analysis of variance (ANOVA) will be apply to determine the intervention effect over the time 0, 30 day, 60 day, 90 day, and 120 day). P significance was set up ≤ 0.05.

Interventions

OTHEROrange juice

Thirty days before the beginning of trial, women (n= 10; BMI 23.8 kg/m2; 28 years) will be advised to not consumed foods containing prebiotic, probiotic and fibers, and citrus fruits and beverages. After 30 days, the participants will consume 300 mL of orange juice daily during 60 days. After 60 days of orange juice intervention, the participants will be submitted to 30 days of washout. Samples of blood, urine and feces will collect in five different occasions (baseline, 30 day, 60 day, 90 day, and 120 day) in order to evaluate the prebiotic effect of orange juice on gut microbiota and the bioavailability of its flavanones in blood, urine and feces.

Sponsors

São Paulo State University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

Healthy women BMI 18.5 - 29.9 kg/m2.

Exclusion criteria

Gastrointestinal diseases Pregnant women Regular use of medications Dietary restrictions, vegetarian diet, macrobiotic, etc. Use of vitamins or dietary supplements Use of probiotics or prebiotics in the last 3 months and antibiotics in the last 6 months.

Design outcomes

Primary

MeasureTime frame
Total counting of aerobic bacteria and facultative anaerobic bacteria4 months
Determination of butyric acid4 months
Determination of acetic acid4 months
Ammonium concentration4 mounths

Secondary

MeasureTime frameDescription
% body fat4 months
Ratio waist/hip4 mounths
Glucose4 mounths
Insulin4 mounths
Total cholesterol4 mounths
Low density lipoprotein cholesterol4 mounths
High density lipoprotein cholesterol4 mounths
Bioavailability of hesperitin and naringenin in the blood, urine and feces4 monthsQuantification of hesperidin and naringenin and identification and quantification of their metabolites in the blood, urine and feces
hsCRP4 mounths
Alkaline phosphatase4 mounths
Aspartate enzyme aminotransferase4 mounths
Alanine enzyme aminotransferase4 mounths
GammaGT4 mounths
Glycemic curve4 mounths
Insulin curve4 mounths
Triglycerides4 mounths
Body mass index4 months
Body lean mass4 months
Body fat mass4 months

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026