Beneficial Impact of Orange Juice Consumption on Risk Factors Associated With Cardiovascular Diseases

Cardiovascular Risk Factors Clinical Trial

— CITRUS  

Official title:

Randomized, Parallel and Double Blind Placebo-controlled Study for the Evaluation of Both Acute and Chronic Role of Hesperidin Consumption in 100% Orange Juice

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02479568
• Other study ID #: CITRUS 14-12
• Status: Completed
• Phase: Phase 3
• Start date: January 12, 2016
• Est. completion date: July 6, 2017

Study information

• Verified date: February 2022
• Source: Technological Centre of Nutrition and Health, Spain
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary aim is to examine both the acute and chronic effects of hesperidin consumption from 100% Florida orange juice in various doses on functional and systemic markers associated with cardiovascular disease (CVD) risks.

Description:

The aim of this study is to compare the effect of different doses of hesperidin in 100% Florida orange juice (OJ) when regularly or postprandially consumed on cardiovascular risk markers; in addition, the plausible role and mechanism of the hesperidin will be investigated.

The sample size was calculated using a previously available bibliography using systolic blood pressure (SBP) as the primary outcome measure. A total of 84 subjects per study product group were needed, assuming variance components of approximately 20.0, to detect differences between the three groups (control, orange juice and hesperidin-enriched orange juice (10 mm Hg)) with a bilateral significance level of α=0.05 and a power of 80 %.

The sample size was computed to be sufficient to detect differences between treatment groups regarding the evolution in time of SBP levels. Justification of chosen sample size is based on the clinically meaningful difference assigned to δ=10.0 mm Hg, which is equivalent to a difference of approximately 7.4 % in patients with baseline SBP levels of approximately 135 mm Hg. Thus, a sample of 252 participants can be used for the chronic three arm parallel trial design (84 subjects/arm) and will allow us to detect small but clinically relevant differences between the three groups with statistical robustness and direct interpretation in terms of the chronic treatment effect.

To the acute postprandial tests, the investigators have chosen n=20 subjects per arm according to the most studies that have addressed the metabolic effects of a postprandial intervention have been performed using a very similar number of subjects with statistically good quality results.

The statistical analysis will follow the principles specified in the guidelines of the ICHE9 and CPMP/EWP/908/99 ICHE9 Points to Consider on Multiplicity Issues in Clinical Trials.

The continuous efficacy variables will be analyzed by an ANCOVA (analysis of covariance) with the baseline value as a covariate.

The efficacy outcomes will be determined using the absolute values and absolute differences from the baseline. The efficacy analysis will be performed using the Available Data Only approach. In addition, the analysis of the primary efficacy variable will be performed with the Baseline Observation Carried Forward approach.

A suitable hypothesis test will be applied to the rest of the variables according to the nature of each variable, such as the Fisher exact test for categorical variables, Student's T-test for continuous variables and Mann-Whitney U test for ordinal scale variables.

The statistical tests will be applied with an α=0.05 two-sided significance level. Post-hoc analyses and comparisons between pairs of groups will be done as for exploratory purposes.

In addition, the statistical plan will be transferred to the application form of the electronic data collection report (e-CDR), which allows the improvement of data management, diminishes human errors (according threshold values of each outcome) and, overall, guarantees the maximum exploitation of human data in the context of statistical analysis.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 159
• Est. completion date: July 6, 2017
• Est. primary completion date: July 6, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion criteria

• Men or women 18-65 years old

• No evidence of chronic disease

• No familial CVD history

• Written informed consent provided before the initial screening visit.

• Blood pressure (with no drug intervention) >120 mm Hg systolic blood pressure = 159 mmHg

Exclusion criteria

• Body mass index (BMI) = 35 kg/m2

• Glucose >125 mg/dl

• Systolic blood pressure = 160 mm Hg and diastolic blood pressure >100 mm Hg or taking antihypertensive medications

• Total cholesterol >240 mg/dl

• LDL-cholesterol >160 md/dl

• TAG >350

• Smoking

• Pregnant or intending to become pregnant

• Use of medications, antioxidants, or vitamin supplements

• Chronic alcoholism

• Intense physical activity (5h/week)

• Intestinal disorders

• Following of a vegetarian diet

• Anemia (hemoglobin =13 g/dL in men and =12 g/dL in women)

• Current or past participation in a clinical trial or consumption of a research product in the 30 days prior to inclusion in the study

• Failure to follow the study guidelines.

Related Conditions & MeSH terms

• Cardiovascular Diseases
• Cardiovascular Risk Factors

Intervention

Dietary Supplement:
• Control
500 mL (250 mL; 2 times/day) of placebo drink for 12 weeks
• 100% Florida OJ
500 mL (250 mL; 2 times/day) of 100% Florida OJ for 12 weeks
• 100% Florida OJ-enriched
500 mL (250 mL; 2 times/day) of 100% Florida OJ-enriched for 12 weeks

Locations

Country	Name	City	State
Spain	Technological Centre of Nutrition and Health (CTNS)	Reus	Tarragona

Sponsors (5)

Lead Sponsor	Collaborator
Technological Centre of Nutrition and Health, Spain	Florida Department of Citrus, Hospital Universitari Sant Joan de Reus, Technological Centre of Nutrition and Health, University Rovira i Virgili

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Transcriptomics	Plasma collected at 0 h (V1 and V7) of 20 samples each arm (volunteers in the postprandial study). These cells will be used to perform transcriptomics analysis to detect whole gene expression changes due to the chronic consumption of two doses of hesperidin in 100% Florida orange juice.	At week 0 (V1) and 12 week (V7).
Other	Non-targeted Metabolomics	Plasma collected at 0 h (V1 and V7) of 20 samples each arm (volunteers in the postprandial study) will be used to perform non-targeted metabolomics by Nuclear Magnetic Response Spectroscopy (NMR) to detect metabolomic profile changes due to the chronic consumption of two doses of hesperidin in 100% Florida orange juice	At week 0 (V1) and 12 week (V7).
Primary	Systolic Blood Pressure	During each visit, SBP will be measured after 5 min in a seated position in a comfortable room by the physician. The measurement will be taken in duplicate at 1-min intervals using an automatic sphygmomanometer (OMRON HEM-907; Peroxfarma, Barcelona, Spain), and the average of the two measurements will be calculated.	Every 2 weeks for a total of 12 weeks.
Secondary	Diastolic Blood Pressure	During each visit, diastolic BP will be measured after 5 min in a seated position in a comfortable room by the physician. The measurement will be taken in duplicate at 1-min intervals using an automatic sphygmomanometer (OMRON HEM-907; Peroxfarma, Barcelona, Spain), and the average of the two measurements will be calculated.	Every 2 weeks for a total of 12 weeks.
Secondary	Ischemic reactive hyperemia (IRH)	The endothelial-dependent vasomotor functions will be measured as IRH by a Laser-Doppler linear Periflux 5000 flowmeter (Perimed AB, Järfälla, Stockholm, Sweden)	Every 4 weeks for a total of 12 weeks
Secondary	Platelet aggregation	Multiplate analyzer, Roche	Every 4 weeks for a total of 12 weeks
Secondary	Homocysteine	Homocysteine concentrations will be measured by liquid chromatography-mass spectrometry (LC-MS/MS)	Every 4 weeks for a total of 12 weeks
Secondary	C-reactive protein (inflammatory marker)	High sensitivity C-reactive protein (hsCRP) by standardized methods in a Cobas Mira Plus autoanalyzer (Roche Diagnostics Systems, Madrid, Spain)	Every 4 weeks for a total of 12 weeks
Secondary	oxidized LDL (as oxidative stress biomarker)	Mercodia Oxidized LDL ELISA kit will be used to measure the oxidized LDL (mU/L).	Every 4 weeks for a total of 12 weeks

External Links

•   Florida Department of Citrus
•   Technological Centre of Nutrition and Health