Clinical TrialID 5609

FLAVIOLA Health Study

NCT01799005

Vascular Health

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
5609
Evidence Id
5609
Core Evidence Id
5609
Source Clinical Trial Id
5593
Herb2 Clinical Trial Id
HBCT005593
Nct Id
NCT01799005
Title
FLAVIOLA Health Study
Status
Completed
Phase
Study Result
No
Study Condition
Vascular Health
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: PREVENTION
Intervention
DIETARY_SUPPLEMENT: Flavanol (410 mg)|DIETARY_SUPPLEMENT: Control (no flavanols)
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Quadruple
Intervention Purpose
Prevention
Gender
All
Age
Adult
Enrollment
100
Outcome Measure
Endothelial function, Time points: day 0 [baseline], and day 30 each 0 and 2h.
Sponsor Collaborator
Heinrich-Heine University, Duesseldorf
Funded By
OTHER
Location
Division of Cardiology, Pulmonology and Vascular Medicine, Duesseldorf, NRW, 40225, Germany
Other Id
FHS
Start Date
2013-02
Primary Completion Date
2014-08
Completion Date
2014-08
First Posted
2013-02-26
Results First Posted
Last Update Posted
2015-02-03
Study Document
Study Url
https://clinicaltrials.gov/study/NCT01799005
Title Cn
Title En
FLAVIOLA Health Study
Bilingual Status
semi_complete