Department of Clinical Pharmacology, Institute of Public Health, University of Southern Denmark
Odense C, DK-5000, Denmark
NCT Number: NCT01921881
The goal of the study is to examine if healthy individuals that ingest St John's wort will have a significantly difference in glucose tolerance.
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Notify Me18 year–40 year
Male
Interventional
Phase 1
Odense C, DK-5000, Denmark
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Glucose concentration 0, 15, 30, 45, 60, 90 and 120 after glucose ingestion
At time=0, the subjects will ingest 75g glucose. Plasma glucose will be measured at 0, 15, 30, 45, 60, 90 and 120 minutes after glucose ingestion.
Time frame: At time=0
At time=0, the concentration of active components hypericin and hyperforin will be measured.
Time frame: At time points, 0, 15, 30, 45, 60, 90, 120 minutes after glucose ingestion
C-peptide and serum insulin will also be measured during the oral glucose tolerance test.
University of Southern Denmark
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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