Clinical Trials Directory

Trials / Completed

CompletedNCT04316390

Influence of Hesperidin and Vitamin C on Uric Acid Concentration

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
University of Kiel · Academic / Other
Sex
All
Age
20 Years – 80 Years
Healthy volunteers
Accepted

Summary

Aim of the study is to investigate the impact of hesperidin and/or vitamin C on elevated uric acid concentrations.

Detailed description

Duration of the study is 9 weeks. 1) a washout week, 2) two intervention weeks, 3) four weeks washout period, 4) two intervention weeks. The study is conducted under free living conditions. During washout weeks consumption of orange juice or citrus fruits or vitamin C containing supplements is restricted. During intervention weeks 200 mL of study drink is consumed daily. And participants are asked to maintain their normal physical activity and habitual diet. Additional citrus or vitamin C containing beverages are not allowed. At the beginning and the end of each intervention phase uric acid, insulin sensitivity, blood pressure, pulse wave velocity and bioavailability of hesperidin are assessed.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTControlstudy drink (two weeks)
DIETARY_SUPPLEMENTHesperidinstudy drink + Hesperidin 600 mg (two weeks)
DIETARY_SUPPLEMENTVitamin Cstudy drink + Vitamin C 250 mg (two weeks)
DIETARY_SUPPLEMENTHesperidin + Vitamin Cstudy drink + Hesperidin 600 mg + Vitamin C 250 mg (two weeks)

Timeline

Start date
2022-07-15
Primary completion
2023-03-22
Completion
2023-03-30
First posted
2020-03-20
Last updated
2023-07-03

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT04316390. Inclusion in this directory is not an endorsement.