Efficacy and Safety of Zingiber Officinale Roscoe Extract on Body Fat
NCT ID: NCT03260751
Last Updated: 2019-05-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
80 participants
INTERVENTIONAL
2017-02-03
2018-01-29
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
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Zingiber officinale Roscoe extract 200 mg
2 cap/day, 800 mg/cap for 12 weeks
Zingiber officinale Roscoe extract 200 mg
2 cap/day, 800 mg/cap for 12 weeks
Placebo
Placebo for 12 weeks
Placebo
Placebo for 12 weeks
Interventions
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Zingiber officinale Roscoe extract 200 mg
2 cap/day, 800 mg/cap for 12 weeks
Placebo
Placebo for 12 weeks
Eligibility Criteria
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Inclusion Criteria
* BMI 25\~29.9 kg/m2
* subjects giving written informed consent
Exclusion Criteria
* Cardiovascular disease, e.g. arrhythmia, heart failure, myocardial infarction, and patient with pacemaker
* History of disease that could interfere with the test products or impede their absorption, such as gastrointestinal disease or gastrointestinal surgery
* Participation in any other clinical trials within past 2 months
* Laboratory test, medical or psychological conditions deemed by the investigators to interfere with successful participation in the study
* Pregnancy or breast feeding etc,.
19 Years
65 Years
ALL
Yes
Sponsors
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Chonbuk National University Hospital
OTHER
Responsible Party
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Soo-Wan Chae
Principal investigator, Clinical Trial Center for Functional Foods
Locations
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Clinical Trial Center for Functional Foods Chonbuk National University Hospital
Jeonju, Jeollabuk-do, South Korea
Countries
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Other Identifiers
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WJ-BF-ZO
Identifier Type: -
Identifier Source: org_study_id
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