ConductScience.org, home

Trial · NCT07890987

VISION Study: Visualization-Guided SMAS Treatment to Optimize Nonsurgical Lifting

NCT07890987, Not applicable, Recruiting, Ocean Clinic

3 sourcestrials-2026-11-12-0.5.0

Download JSON
Cite this record

ConductScience Library. VISION Study: Visualization-Guided SMAS Treatment to Optimize Nonsurgical Lifting. Trials, record NCT07890987. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07890987

On this page

Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
VISION Study: Visualization-Guided SMAS Treatment to Optimize Nonsurgical Lifting
NCT number
NCT07890987
Status
Recruiting
Phases
Not applicable
Enrollment
50 participants, estimated
Lead sponsor
Ocean Clinic
Conditions
Facial Skin Laxity
Interventions
Microfocused Ultrasound with Visualization (MFU-V), multi Microfocused Ultrasound with Visualization (MFU-V)
First posted
2026-10-23
Last updated
2026-10-23

Source ClinicalTrials.gov

Registered outcomes12

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange in SMAS/Fibromuscular Layer FirmnessBaseline and Day 180Difference between baseline and Day 180 in SMAS/fibromuscular layer stiffness measured using Shear-Wave Elastography.
SecondaryChange From Baseline in Facial Soft-Tissue Displacement Measured by Vectra 3D ImagingBaseline, Day 90, and Day 180
Facial tissue displacement, in millimeters (mm), measured by three-dimensional imaging with the Vectra 3D system (Canfield Scientific), compared between the single-depth (1.5 mm) side and the multi-depth side. Time Frame : Baseline, Day 90, and Day 180
Secondarychanges in dermal thicknessBaseline and Day 180Histologic evaluation of treatment-induced change in dermal thickness. Unit of Measure: millimeters (mm)
SecondaryChange in Skin elasticity measured by ElastiMeterBaseline, Day 90, and Day 180
Instant skin elasticity (ISE), expressed in newtons per meter (N/m), measured by indentation with the ElastiMeter (Delfin Technologies) on each side of the face. Higher values indicate greater tissue resistance to indentation. Compared between the single-depth (1.5 mm) side and the multi-depth side.
SecondaryChange in collagen type I regenerationBaseline and Day 180
Histologic evaluation of collagen type I regeneration measured by immunohistochemistry, expressed as the percentage of collagen-I-positive area relative to total tissue area. Unit of Measure: % positive area
SecondaryChange in collagen type III regenerationBaseline and Day 180
Histologic evaluation of collagen type III regeneration measured by immunohistochemistry, expressed as the percentage of collagen-III-positive area relative to total tissue area. Unit of Measure: % positive area
SecondaryChange in elastin regenerationBaseline and Day 180
Histologic evaluation of elastin regeneration measured by elastin-specific staining/immunohistochemistry, expressed as the percentage of elastin-positive area relative to total tissue area. Unit of Measure: % positive area
SecondaryChange in proteoglycan contentBaseline and Day 180
Histologic evaluation of proteoglycan content measured by Alcian Blue/Safranin O staining or proteoglycan-specific immunohistochemistry, expressed as the percentage of stained area relative to total tissue area. Unit of Measure: % positive area
SecondaryChange in collagen fiber alignmentbaseline and day 180
image-analysis-derived collagen fiber coherence/alignment, expressed as an orientation index ranging from 0 (random alignment) to 1 (perfect alignment). Unit of Measure: orientation index (0-1), dimensionless
SecondaryChange in elastin fiber alignmentBaseline and day 180
Image-analysis-derived elastin fiber coherence/alignment, expressed as an orientation index ranging from 0 (random alignment) to 1 (perfect alignment). Unit of Measure: orientation index (0-1), dimensionless

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.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
38773827BACKGROUND

Source PubMed

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT07890987

GET https://conductscience.org/api/trials/v1/NCT07890987/registered