Clinical TrialID 847

Efficacy and Safety Morus Alba L. Extract on Improvement of Blood Flow

NCT03807570

Blood Flow

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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
847
Evidence Id
847
Core Evidence Id
847
Source Clinical Trial Id
829
Herb2 Clinical Trial Id
HBCT000829
Nct Id
NCT03807570
Title
Efficacy and Safety Morus Alba L. Extract on Improvement of Blood Flow
Status
Phase
Study Result
No
Study Condition
Blood Flow
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: PREVENTION
Intervention
DIETARY_SUPPLEMENT: Morus Alba L. Extract|DIETARY_SUPPLEMENT: Placebo
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Double
Intervention Purpose
Prevention
Gender
All
Age
Adult, Older_Adult
Enrollment
100
Outcome Measure
Changes of Reactive Hyperemia Index, Reactive Hyperemia Index was measured in study visit 1(0 week) and visit 3(12 weeks)., 12 weeks|Changes of Platelet function assay, The whole blood with anticoagulant (sodium citrate) is passed through the capillary and the membrane to assess the degree of platelet adhesion to this membrane and the degree of occlusion of the capillary., 12 weeks
Sponsor Collaborator
Chonbuk National University Hospital
Funded By
OTHER
Location
Clinical Trial Center for Functional Foods Chonbuk National University Hospital, Jeonju, Jeollabuk-do, 54907, Korea, Republic of
Other Id
BA-BF-MBE
Start Date
2018-11-12
Primary Completion Date
2021-01-30
Completion Date
2021-01-31
First Posted
2019-01-17
Results First Posted
Last Update Posted
2020-05-08
Study Document
Study Url
https://clinicaltrials.gov/study/NCT03807570
Title Cn
Title En
Efficacy and Safety Morus Alba L. Extract on Improvement of Blood Flow
Bilingual Status
semi_complete