Trial · NCT07896993
Mask Instant Clinical Study
NCT07896993, Not applicable, Completed, ChinaNorm
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Mask Instant Clinical Study. Trials, record NCT07896993. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07896993
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Mask Instant Clinical Study
- NCT number
- NCT07896993
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 35 participants, actual
- Lead sponsor
- ChinaNorm
- Conditions
- Skin Barrier Function, Skin Soothing Effect
- Interventions
- Test soothing facial mask
- First posted
- 2026-10-27
- Last updated
- 2026-10-27
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Erythema index measured by Mexameter MX18 | BL (before infrared induction), T0 (immediately after induction), 10 minutes, 1 hour and 2 hours after induction | Skin erythema index of the hemiface will be measured by Mexameter MX18. Three consecutive valid readings will be taken and averaged for each measurement. |
| Secondary | Dermatologist clinical assessment of skin redness | BL (before infrared induction), T0 (immediately after induction), 10 minutes, 1 hour and 2 hours after induction | Dermatologists perform clinical assessment of skin redness using modified Griffiths 10-point scale (0-9, half-point increments allowed). Whenever possible, the same dermatologist assesses the same participant; the rater is not permitted to refer to previous scores for post-baseline evaluations. |
| Secondary | VISIA-CR facial photography | BL (before infrared induction), T0 (immediately after induction), 10 minutes, 1 hour and 2 hours after induction | Standardized facial images (front, left, right) are captured under 4 lighting modes including standard light 1, standard light 2, cross polarized and parallel polarized light. |
| Secondary | TiVi700 measurement of skin microcirculation | BL (before infrared induction), T0 (immediately after induction), 10 minutes, 1 hour and 2 hours after induction | TiVi700 captures skin microvascular red blood cell concentration (TiVi index) on bilateral cheek regions to assess cutaneous microcirculation status. |
| Secondary | Subject self-assessment questionnaire for skin sensory symptoms | 10 minutes, 1 hour and 2 hours after infrared induction | Subjects self-grade stinging, itching, burning and tightness on a 0-4 intensity scale. Score 0 = none; Score 1 = very slight; Score 2 = slight; Score3 = moderate; Score4 = severe. |
| Other | Facial skin temperature measured by FLUKE TiS60+ infrared thermal camera | BL (before infrared induction), T0 (immediately after induction), 10 seconds, 1 minute and 5 minutes after induction | Infrared thermal facial photos are captured to record hemiface skin temperature by trained technicians. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07896993
GET https://conductscience.org/api/trials/v1/NCT07896993/registered