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NCT03759743 Clinical Trial

Evaluate the Efficacy and Safety of LMT1-48 on Reducing Body Fat in Overweight Subject

Overweight Clinical Trial

Official title:
a Randomised, Double Blind, Placebo Controlled Study to Evaluate the Efficacy and Safety of LMT1-48 on Reducing Body Fat in Overweight Subject

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03759743
Other study ID # MT13-KR17OWT712
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 4, 2018
Est. completion date January 7, 2020

Study information
Verified date July 2020
Source Medy-Tox
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the safety and efficacy of LMT1-48(Probiotics) compared to a placebo in reducing the body fat in overweight subjects

Recruitment information / eligibility
Status Completed
Enrollment 97
Est. completion date January 7, 2020
Est. primary completion date August 17, 2019
Accepts healthy volunteers No
Gender All
Age group 19 Years to 70 Years
Eligibility Inclusion Criteria:

- Age between 19 and 70 years

- Overweight (25 kg/m2 = body mass index (BMI) < 30 kg/m2)

Exclusion Criteria:

- Pregnancy or breast-feeding

- Unstable body weight (body weight change > 10% within 3 months before screening)

Study Design

Related Conditions & MeSH terms

Intervention

Dietary Supplement:
• LMT1-48
capsules containing Probiotics
• Placebo
capsules that did not contain any probiotics

Locations
Country Name City State
Korea, Republic of Seoul National University Bundang Hospital Seongnam-si

Sponsors (1)
Lead Sponsor Collaborator
Medy-Tox

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary change from baseline fat percentage at 12 week the body composition of the subjects was measured via dual-energy X-ray absorptiometry (DEXA) to determine at baseline and 12-week follow-up
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