Bioavailability of quercetin in healthy men and wome

Not Applicable

• Conditions: healthy participants

• Registration Number: DRKS00004350
• Lead Sponsor: niversität BonnIEL Ernährungsphysiologie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2012-08-29
• Study Completion: 2012-10-11
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 12

Inclusion Criteria

Healthy, normal-weight, non-smoking

Exclusion Criteria

smoking, overweight/obesity, intake of drugs or dietary supplements, metabolic and endocrine diseases, malabsorption syndromes, alcohol abuse

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
concentration of quercetin in plasma (before bolus intake and after 0,5, 1, 1,5, 2, 3, 4, 5, 6, 7, 8, 9, 24 h)

Secondary Outcome Measures

Name	Time	Method
not defined