Clinical TrialID 329
Red Clover Botanical Dietary Supplements - Metabolism and Safety in Women
NCT03205787
Food-drug Interaction
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Trial: 1Herb: 1Links: 1
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 329
- Evidence Id
- 329
- Core Evidence Id
- 329
- Source Clinical Trial Id
- 315
- Herb2 Clinical Trial Id
- HBCT000315
- Nct Id
- NCT03205787
- Title
- Red Clover Botanical Dietary Supplements - Metabolism and Safety in Women
- Status
- Completed
- Phase
- Study Result
- No
- Study Condition
- Food-drug Interaction
- Study Type
- Interventional
- Study Design
- Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: OTHER
- Intervention
- DIETARY_SUPPLEMENT: Trifolium pratense
- Intervention Allocation
- Intervention Model
- Single_Group
- Intervention Mask
- Intervention Purpose
- Other
- Gender
- Female
- Age
- Adult, Older_Adult
- Enrollment
- 20
- Outcome Measure
- Area Under the Curve (AUC), Concentrations of probe drugs from blood draws at the conclusion of the 14-day intervention were used to calculate areas under the (extrapolated) concentration-time curve to determine any changes compared to pre-intervention., baseline and 14 days
- Sponsor Collaborator
- University of Illinois at Chicago
- Funded By
- OTHER
- Location
- University of Illinois at Chicago, Chicago, Illinois, 60612, United States
- Other Id
- 2017-0436
- Start Date
- 2017-09-21
- Primary Completion Date
- 2020-04-29
- Completion Date
- 2020-07-01
- First Posted
- 2017-07-02
- Results First Posted
- Last Update Posted
- 2021-05-06
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT03205787
- Title Cn
- Title En
- Red Clover Botanical Dietary Supplements - Metabolism and Safety in Women
- Bilingual Status
- semi_complete