Clinical Trials Directory

Trials / Completed

CompletedNCT01667224

Efficacy and Safety of Actiponin on Antiobesity in Obese Korean Subjects.

Actiponin Supplementation Reduces Abdominal Fat Area, Weight, Body Fat Mass and BMI in Obese Korean Subjects.

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Chonbuk National University Hospital · Academic / Other
Sex
All
Age
19 Years – 65 Years
Healthy volunteers
Accepted

Summary

Obesity is a major health issue worldwide; there is a constant raise in obesity related death each year. In vitro and animal studies elucidated Actiponin as a novel anti-obesity agent. However, the efficacy and safety of Actiponin supplementation on body weight regulation in humans are lacking.

Detailed description

The primary aim of the study was to investigate the effect of Actiponin in Korean subjects on body weight and fat loss along with changes in metabolic markers based on 12 week, randomized, double-blind, placebo-controlled clinical trial. Eighty obesity subjects with BMI \> 25kg/m2 and waist-hip ratio (WHR) ≥ 0.90 for men and ≥ 0.85 for women were randomly divided into either Actiponin (n=40, 450mg/day) or placebo group (n=40, 450mg/day) for 12weeks.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTActiponinThe dried leaves of G. pentaphyllum leaves were extracted with 50% ethanol and filtered; the filtrate was concentrated under high pressure and high temperature. Damulin An and B, analytical marker of Actiponin, exist more 2.49% and 1.06% respectively in raw material.
DIETARY_SUPPLEMENTPlaceboAmount and calorie of placebo are same with Actiponin.

Timeline

Start date
2009-10-01
Primary completion
2010-08-01
Completion
2010-10-01
First posted
2012-08-17
Last updated
2017-02-23
Results posted
2014-04-21

Source: ClinicalTrials.gov record NCT01667224. Inclusion in this directory is not an endorsement.