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Study to Investigate the Effect of Superba Boost on the Skin.

NCT04013945 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2023-02-01

No results posted yet for this study

Summary

Study to determine the effect of 12 weeks daily consumption of Superba Boost as compared to placebo on changes in Trans-Epidermal Water-Loss (TEWL).

Conditions

  • Physiology, Skin

Interventions

DIETARY_SUPPLEMENT

Superba Boost (Active)

To assess changes in Trans-epidermal water loss (TEWL), measured at baseline and after 12 weeks of daily consumption with Superba Boost.

DIETARY_SUPPLEMENT

Vegetable oil (Placebo)

To assess changes in Trans-epidermal water loss (TEWL), measured at baseline and after 12 weeks of daily consumption with Placebo.

Sponsors & Collaborators

  • Atlantia Food Clinical Trials

    collaborator INDUSTRY

  • Aker BioMarine Human Ingredients AS

    lead INDUSTRY

Principal Investigators

  • Aoife Hayes, PhD · Atlantia Food Clinical Trials

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-03-13
Primary Completion
2019-08-12
Completion
2020-03-22

Countries

  • Ireland

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 NCT04013945 on ClinicalTrials.gov