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Clinical Trials/NCT01734005
NCT01734005CompletedNot Applicable

Efficacy and Safety of Red Ginseng on Decrement of Body Fat

Chonbuk National University Hospital1 site in 1 country60 target enrollmentStarted: October 10, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
60
Locations
1
Primary Endpoint
Changes in Percent Body Fat

Study Overview

Brief Summary

The investigators performed a 12-week, randomized, double-blind, placebo-controlled human trial to evaluate the efficacy and safety of red ginseng on decrement of body fat. The investigators measured decrement of body fat parameters , including Body Fat Mass, Percent Body Fat, weight and BMI(body mass index), and monitored their blood pressure.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
19 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Males and females 19-65 years old
  • •BMI(body mass index) ≥ 25 kg/m^2 or WC(Waist Circumference) ≥ 90(men), WC ≥ 85(women)
  • •Able to give informed consent

Exclusion Criteria

  • •Significant variation in weight(more 10%) in the past 3 months
  • •Allergic or hypersensitive to any of the ingredients in the test products
  • •History of reaction to any of the test products or of gastrointestinal diseases such as Crohn's disease or gastrointestinal surgery
  • •History of alcohol or substance abuse
  • •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
  • •Pregnant or lactating women etc.

Arms & Interventions

Placebo

Placebo Comparator

Intervention: Placebo (Dietary Supplement)

Red Ginseng

Experimental

Intervention: Red Ginseng (Dietary Supplement)

Outcomes

Primary Outcomes

Changes in Percent Body Fat

Time Frame: 12 weeks

Percent Body Fat was measured in study visit 1(0 week) and visit 3(12 week).

Changes in Body Fat Mass

Time Frame: 12 weeks

Body Fat Mass was measured in study visit 1(0 week) and visit 3(12 week).

Secondary Outcomes

  • Changes in weight(12 weeks)
  • Changes in BMI(body mass index)(12 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Soo-Wan Chae

Principal Investigator, Clinical Trial Center for Functional Foods

Chonbuk National University Hospital

Study Sites (1)

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