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Clinical Trials/NCT07177274
NCT07177274Active, not recruitingNot Applicable

Evaluation of Skin Stiffness Changes in Wounds Before and After Low-Level Laser Therapy Using 660 nm Laser: A Comparative Analysis With OCT and MyotonPRO

Asia University1 site in 1 country20 target enrollmentStarted: September 19, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
20
Locations
1
Primary Endpoint
To evaluate changes in skin stiffness of wound tissue before and after LLLT using OCT and MyotonPRO.

Study Overview

Brief Summary

Chronic wounds and impaired healing remain a major clinical challenge, particularly in patients with diabetes, vascular disease, or age-related skin fragility. Low-level laser therapy (LLLT) at 660 nm has been reported to enhance tissue repair, reduce inflammation, and promote angiogenesis. However, the biomechanical properties of wound tissue following LLLT remain poorly understood.

Optical Coherence Tomography (OCT) provides a non-invasive, high-resolution method to assess skin microstructure and elasticity, while the MyotonPRO offers quantitative stiffness measurements at the tissue surface. Combining these two complementary modalities may provide a more comprehensive assessment of wound healing progression and treatment response.

This study aims to evaluate changes in wound stiffness before and after 660 nm LLLT and to compare them against contralateral normal skin, thereby providing objective insight into the biomechanical efficacy of laser treatment.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Factorial
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •presented chronic and burn wounds lasting more than four weeks.
  • •had partial-thickness burn wounds.

Exclusion Criteria

  • •current smokers.
  • •wounds that were fresh and still bleeding.

Arms & Interventions

Skin status (normal, wound, after treatment)

Active Comparator

Using 660 nm LLLT efficacy on the wound, separated categories into the upper limb and lower limb.

Intervention: Low Level Laser Therapy (Radiation)

Skin location (upper limb, lower limb)

Active Comparator

Using 660 nm LLLT efficacy on the wound, separated categories into the upper limb and lower limb.

Intervention: Low Level Laser Therapy (Radiation)

Outcomes

Primary Outcomes

To evaluate changes in skin stiffness of wound tissue before and after LLLT using OCT and MyotonPRO.

Time Frame: 1 year

Secondary Outcomes

  • To compare wound skin stiffness with contralateral normal skin.(1 year)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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