Clinical Trials Directory

Trials / Completed

CompletedNCT03205787

Red Clover Botanical Dietary Supplements - Metabolism and Safety in Women

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
University of Illinois at Chicago · Academic / Other
Sex
Female
Age
40 Years – 79 Years
Healthy volunteers
Accepted

Summary

Human safety studies were carried out to test whether red clover botanical dietary supplements used by peri- and post-menopausal women are safe to use with Food and Drug Administration (FDA)-approved drugs. To test this, a red clover dietary supplement (previously tested in women at the University of Illinois at Chicago without any harmful effects) was given with four selected FDA-approved drugs to determine if the red clover supplement can increase or decrease how these medications are absorbed, metabolized and excreted by the human body. Preclinical studies predicted that the red clover supplement might affect the metabolism or break down of these probe drugs.

Detailed description

At the start of a study, subjects were administered low doses of a mixture of four FDA-approved drugs (caffeine, tolbutamide, dextromethorphan, and alprazolam), and serial blood samples were drawn and analyzed for the concentration of each drug over time. Afterwards, participants took the red clover dietary supplement twice orally daily for 14 days to allow for potential inhibition or induction of drug metabolizing enzymes and transporters. Thereafter, the same drugs were taken again to obtain a second measure of drug concentrations in blood over time. Changes in the concentration-time curve values for each probe drug obtained before and after ingestion of the supplement were evaluated to determine if metabolism of the probe drugs was impacted by the red clover dietary supplement.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTTrifolium pratenseRed Clover extract standardized to isoflavone content.

Timeline

Start date
2017-09-21
Primary completion
2020-04-29
Completion
2020-07-01
First posted
2017-07-02
Last updated
2021-05-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03205787. Inclusion in this directory is not an endorsement.