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An 8-week Full Face HUT Clinical Trial for HydroBoost (2.0/3.0)

NCT03264677 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 122

Last updated 2018-04-11

No results posted yet for this study

Summary

* To investigate the product regiments' performance on moisturization related skin healthy signs (skin moisturization, barrier function, elasticity, translucency, roughness and skin conditions) through instrumental evaluation, clinical grading and self-assessment before, during and after 8 weeks' home usage under city environmental aggressors (Sun, change of temperature and humidity, wind and air pollution) among 3 product regimens and Non-treatment control;
* To explore the linkage among products efficacy, ambient aggressors, and life habits;
* To investigate product regimens' tolerance and safety via Home Use Test;
* To collect skin microflora/microbiome samples for potential research on skin microbiome distribution change as impacted by product application and/or environmental aggressors change (data will be analyzed and reported separately).

Conditions

  • Adult Skin Healthy Signs

Interventions

COMBINATION_PRODUCT

Group 1

NTG Hydro Boost Gelee Milk Cleanser + NTG Hydro Boost Kiwi Water Gel

COMBINATION_PRODUCT

Group 2

NTG Hydro Boost Gelee Milk Cleanser + NTG Hydro Boost Water Gel

COMBINATION_PRODUCT

Group 3

NTG Hydro Boost Gelee Milk Cleanser + NTG Hydro Boost Extra Dry Emulsion

Sponsors & Collaborators

  • Shanghai Skin Disease Hospital

    collaborator UNKNOWN

  • Shanghai China-Norm Management Consulting co.,LTD

    collaborator UNKNOWN

  • Johnson & Johnson Pte Ltd

    lead INDUSTRY

Principal Investigators

  • Chao Yuan · Shanghai Skin Disease Hospital

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-05-18
Primary Completion
2017-07-25
Completion
2017-07-25

Countries

  • China

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 NCT03264677 on ClinicalTrials.gov