Clinical TrialID 8167

Blood Flow Restriction and Creatine Supplementation in Women

NCT05877417

Physical Inactivity

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
8167
Evidence Id
8167
Core Evidence Id
8167
Source Clinical Trial Id
8165
Herb2 Clinical Trial Id
HBCT008165
Nct Id
NCT05877417
Title
Blood Flow Restriction and Creatine Supplementation in Women
Status
Completed
Phase
Study Result
No
Study Condition
Physical Inactivity
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: BASIC_SCIENCE
Intervention
DIETARY_SUPPLEMENT: Creatine Monohydrate|DEVICE: Blood Flow Restriction|OTHER: Exercise
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Double
Intervention Purpose
Basic_Science
Gender
Female
Age
Adult
Enrollment
68
Outcome Measure
Strength, isokinetic dynanometer, Pre, 5-Days post loading, 4wk, 8wk|Body Composition, BIS, BodPod, Pre, 5-Days post loading, 4wk, 8wk|Neuromuscular Function, EMG, Pre, 5-Days post loading, 4wk, 8wk|Endothelial Function, Flow Mediated Dilation, Pre, 5-Days post loading, 4wk, 8wk
Sponsor Collaborator
University of Central Florida
Funded By
OTHER
Location
University of Central Florida, Orlando, Florida, 32816, United States
Other Id
STUDY00005471
Start Date
2023-05-17
Primary Completion Date
2023-12-20
Completion Date
2024-03-01
First Posted
2023-05-26
Results First Posted
Last Update Posted
2024-06-12
Study Document
Study Url
https://clinicaltrials.gov/study/NCT05877417
Title Cn
Title En
Blood Flow Restriction and Creatine Supplementation in Women
Bilingual Status
semi_complete