- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07680309
Evaluation Skin Stiffness Gradient on Skin After LLLT
June 25, 2026 updated by: Gilang Titah Ramadhan, Asia University
Optimization of Low-Level Laser Therapy Via Biomechanical Properties Analysis Using Optical Coherence Tomography on Skin
This study evaluates the effects of Low-Level Laser Therapy (LLLT) on skin elasticity by measuring a 3x3 stiffness gradient across 9 points spaced 1 cm apart.
Using an air-pressure pump integrated with an Optical Coherence Tomography (OCT) system, a deep learning model is utilized to automatically segment and track micro-scale skin movement during deformation.
Study Overview
Status
Active, not recruiting
Conditions
Study Type
Interventional
Enrollment (Estimated)
20
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Wufeng
-
Taichung, Wufeng, Taiwan, 41354
- Asia University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Healthy adult
Exclusion Criteria:
- People with wound and ulcers
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Three different LLLT Duration (2 min, 3 min and 5 min)
Measuring biomechanical changes on skin after LLLT for three different duration (2 min, 3 min and 5 min) using stiffness gradient
|
LLLT intervention on skin biomechanical properties in three different duration and two LLLT wavelength
|
|
Active Comparator: Two different LLLT wavelength (660 and 808 nm)
Measuring biomechanical changes on skin after LLLT for two different LLLT wavelength (660 and 808 nm) using stiffness gradient
|
LLLT intervention on skin biomechanical properties in three different duration and two LLLT wavelength
|
|
Active Comparator: Three different duty cycle (100%, 30% and 50%)
Measuring biomechanical changes on skin after LLLT for three duty cycle (100%, 30% and 50%) using stiffness gradient
|
LLLT intervention on skin biomechanical properties in three different duty cycle and two applied frequency
|
|
Active Comparator: Two different applied frequency (1 Hz and 50 Hz)
Measuring biomechanical changes on skin after LLLT for two different applied frequency (1 Hz and 50 Hz) using stiffness gradient
|
LLLT intervention on skin biomechanical properties in three different duty cycle and two applied frequency
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Measurements skin stiffness gradient
Time Frame: Through study completion, an average of 1 year
|
This study evaluates the effects of Low-Level Laser Therapy (LLLT) on skin elasticity by measuring a 3x3 stiffness gradient across 9 points spaced 1 cm apart.
Using an air-pressure pump integrated with an Optical Coherence Tomography (OCT) system, a deep learning model is utilized to automatically segment and track micro-scale skin movement during deformation.
|
Through study completion, an average of 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 10, 2025
Primary Completion (Actual)
June 15, 2025
Study Completion (Estimated)
August 15, 2026
Study Registration Dates
First Submitted
June 25, 2026
First Submitted That Met QC Criteria
June 25, 2026
First Posted (Actual)
July 2, 2026
Study Record Updates
Last Update Posted (Actual)
July 2, 2026
Last Update Submitted That Met QC Criteria
June 25, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CRREC-112-130/2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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