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Facial Skin Clinical and Microbial Profiling From Oral Probiotic Supplementation

NCT05597254 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 109

Last updated 2023-05-01

No results posted yet for this study

Summary

The goal of this double-blind randomized clinical trial is to investigate the effects on the skin from oral intake of probiotic supplements in healthy adult men and women. The main questions it aims to answer are: • Will probiotic supplementation result in beneficial changes to different skin parameters? • Will probiotic supplementation result in alterations in the skin microbiome? Participants will consume the study product daily for 8 weeks and come in for skin measurements at baseline and after 8 weeks.

Conditions

  • Healthy
  • Skin Manifestations

Interventions

DIETARY_SUPPLEMENT

Probiotic with niacin and berry extract

1 capsule daily of probiotic with niacin supplementation for 8 weeks

DIETARY_SUPPLEMENT

Probiotic without niacin and berry extract

1 capsule daily of probiotic without niacin supplementation for 8 weeks

DIETARY_SUPPLEMENT

Placebo

1 capsule daily of placebo supplementation for 8 weeks

Sponsors & Collaborators

  • Oriflame Cosmetics AB

    lead INDUSTRY

Principal Investigators

  • Isabella Lee · Global Senior Nutritional Scientist

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-09-26
Primary Completion
2022-12-09
Completion
2022-12-09

Countries

  • Sweden

Study Locations

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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 NCT05597254 on ClinicalTrials.gov