Clinical TrialID 970

Evaluation of Soy-protein Russian Tarragon (Artemisia Dracunculus L.)

NCT02088203

Diabetes Prevention

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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
970
Evidence Id
970
Core Evidence Id
970
Source Clinical Trial Id
951
Herb2 Clinical Trial Id
HBCT000951
Nct Id
NCT02088203
Title
Evaluation of Soy-protein Russian Tarragon (Artemisia Dracunculus L.)
Status
Completed
Phase
Phase 1
Study Result
No
Study Condition
Diabetes Prevention
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: PREVENTION
Intervention
DIETARY_SUPPLEMENT: Dose 1|DIETARY_SUPPLEMENT: Dose 2|DIETARY_SUPPLEMENT: Dose 0|DIETARY_SUPPLEMENT: Dose 3|DIETARY_SUPPLEMENT: Dose 4|DIETARY_SUPPLEMENT: Dose 5|DIETARY_SUPPLEMENT: Dose 6
Intervention Allocation
Randomized
Intervention Model
Crossover
Intervention Mask
Double
Intervention Purpose
Prevention
Gender
All
Age
Adult, Older_Adult
Enrollment
64
Outcome Measure
Levels of bioactive components from the Russian Tarragon Nutrasorb in the blood and urine, on average weekly for 3 weeks
Sponsor Collaborator
Pennington Biomedical Research Center|National Center for Complementary and Integrative Health (NCCIH)|Office of Dietary Supplements (ODS)
Funded By
OTHER
Location
Pennington Biomedical Research Center, Baton Rouge, Louisiana, 70808, United States
Other Id
PBRC 2013-049|P50AT002776
Start Date
2014-02
Primary Completion Date
2018-05
Completion Date
2018-05
First Posted
2014-03-14
Results First Posted
Last Update Posted
2019-03-21
Study Document
Study Protocol and Statistical Analysis Plan, https://cdn.clinicaltrials.gov/large-docs/03/NCT02088203/Prot_SAP_000.pdf
Study Url
https://clinicaltrials.gov/study/NCT02088203
Title Cn
Title En
Evaluation of Soy-protein Russian Tarragon (Artemisia Dracunculus L.)
Bilingual Status
semi_complete