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Study of Safety and Efficacy of a Probiotic and Postbiotic in Overweight Individuals

NCT05428137 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 180

Last updated 2024-03-05

No results posted yet for this study

Summary

Investigate the effect of a probiotic (live bacteria) and postbiotic (heat-treated bacteria) strains in overweight individuals.

Conditions

Interventions

DIETARY_SUPPLEMENT

Probiotic

Live bacteria strain in a form of a capsule daily for 16 weeks

DIETARY_SUPPLEMENT

Postbiotic

Heat treated bacteria strain in a form of a capsule daily for 16 weeks

OTHER

Placebo

Placebo in a form of a capsule given for 16 weeks

Sponsors & Collaborators

  • The Archer-Daniels-Midland Company

    lead INDUSTRY

Principal Investigators

  • Daniel Ramon Vidal · ADM Biopolis

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-07-01
Primary Completion
2024-12-31
Completion
2024-12-31

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05428137 on ClinicalTrials.gov