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Not Yet RecruitingNCT07423325

Validation of Skin Instrumentation to Detect Ceramide-Driven Lipid Replenishment - Assessing Skin Glow, Hydration, Trans Epidermal Water Loss, Skin Surface Assessment, Sebum and Least-Reflection Factor.

Validation of Skin Instrumentation to Detect Ceramide-Driven Lipid Replenishment - Assessing Skin Glow, Hydration, Trans Epidermal Water Loss, Skin Surface Assessment, Sebum and Least-Reflection Factor

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
15 (estimated)
Sponsor
NovoBliss Research Pvt Ltd · Academic / Other
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

This is a single-center, open-label, split-face, site-randomized validation study, NB250045-NB-V designed to establish and confirm the reliability, reproducibility, and sensitivity of various skin measurement methods. Evaluator blinding will be implemented to minimize observer bias.

Detailed description

Each subject will serve as their own control, with right side of the face receiving the ceramide-containing moisturizer and the left side receiving water application as the control. This split-face approach reduces inter-subject variability and enables direct intra-individual comparison of the measurement methods across treated and control sites. The study involves a single on-site visit for each subject. * Baseline (pre-application): Subjects will undergo acclimatization in a controlled environment, after which baseline assessments will be performed for skin parameters on both test and control sites. * Application phase: The ceramide-containing moisturizer and water control will be applied to the randomized sites under investigator supervision. * Post-application assessments: Instrumental evaluations will be done at T15 mins following product application.

Conditions

Interventions

TypeNameDescription
OTHERMarketed Product - CeraVe MoisturizerThe test cream was applied topically once daily to the designated treatment area. An adequate amount was gently massaged into clean, dry skin until fully absorbed. Participants were instructed not to wash the treated area for a specified period after application. The application procedure was standardized and followed consistently throughout the study duration.

Timeline

Start date
2026-02-27
Primary completion
2026-02-28
Completion
2026-02-28
First posted
2026-02-20
Last updated
2026-02-20

Source: ClinicalTrials.gov record NCT07423325. Inclusion in this directory is not an endorsement.