- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06489301
Mechanisms for Laser-Induced Rejuvenation
May 18, 2026 updated by: Wright State University
It has shown that laser wounding of geriatric skin protects it against skin cancer.
The purpose of this study is to determine the origin of cells called fibroblasts which are present after treatment with Fractionated Laser Resurfacing (FLR).
These cells restore a youth-like ultraviolet B (UVB) response, but where they come from is currently unknown.
The study recruits subjects who are scheduled to undergo abdominoplasties to investigate the origin of those cells stimulated by laser treatment.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
12
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 Contact
- Name: Manager, Clinical Research Operations
- Phone Number: 937-245-7500
- Email: pturesearch@wrightstatephysicians.org
Study Contact Backup
- Name: Regulatory Specialist
- Phone Number: 937-245-7500
- Email: pturesearch@wrightstatephysicians.org
Study Locations
-
-
Ohio
-
Fairborn, Ohio, United States, 45324
- Recruiting
- Pharmacology Translational Unit
-
Contact:
- Pharmacology Translational Unit
- Phone Number: 937-245-7500
- Email: pturesearch@wrightstatephysicians.org
-
-
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
No
Description
Inclusion Criteria:
- Adult males and females 18 and older
- Able to comprehend procedures and risks
- Planning to undergo abdominoplasty surgery
- Minimum amount of skin to be removed is 50 x 20cm
Exclusion Criteria:
- Medical history of not well-controlled diabetes. This is defined as a subject who needs high doses of insulin, recent history of hospitalization for diabetes-related complications, or poor wound health as evidenced by diabetic ulcers. Subjects who have been deemed healthy enough for abdominoplasty surgery would tend to suggest that their diabetes should not be an issue. However, if the subjects have diabetic complications as outlined above, they could affect the wound healing which is the object of this protocol so they would be excluded.
- Pregnant or nursing
- History of pathologically abnormal wound healing such as keloidal scars
- Existing tattoos on the abdomen that are so extensive that they could interfere with the study
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: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Fractionated Laser Resurfacing
At 14 days prior to scheduled surgery a 5x5cm square on the left abdomen within the region of skin to be excised and treated with fractionated laser resurfacing.
Then at 7 days prior to scheduled surgery a 5 cm diameter circle on the right abdomen within the region of skin to be excised, at least 10 cm away from the square, is treated with fractionated laser resurfacing.
|
A rejuvenating laser that makes tiny holes in the very superficial part of the skin.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
To test if the new fibroblasts that develop in response to fractionated laser resurfacing (FLR) wounding are derived from blood-derived monocytes.
Time Frame: 2 weeks prior to skin removal and 1 week prior to skin removal
|
Identify cells in the skin that have been wounded by FLR at 2 weeks and 1 week previously, for cells that co-express markers for both fibroblasts and monocytes by using single cell RNA-sequencing
|
2 weeks prior to skin removal and 1 week prior to skin removal
|
|
To test if possible cells transitioning from monocytes to fibroblasts are found in the top part of the dermis (papillary dermis).
Time Frame: 2 weeks prior to skin removal and 1 week prior to skin removal
|
Using tissue RNA-seq, PI will define if co-expressing cells are in the papillary dermis.
|
2 weeks prior to skin removal and 1 week prior to skin removal
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
To define the number and types of cells populating the skin following fractionated laser resurfacing (FLR) wounding
Time Frame: 2 weeks prior to skin removal and 1 week prior to skin removal
|
Define the number and types of cells following FLR wounding at 2 weeks and 1 week prior to skin removal by using single-cell RNA-seq.
|
2 weeks prior to skin removal and 1 week prior to skin removal
|
|
To define the locations of the number of cells populating in the skin following fractionated laser resurfacing (FLR) wounding
Time Frame: 2 weeks prior to skin removal and 1 week prior to skin removal
|
Define the locations of the number cell following FLR wounding at 2 weeks and 1 week prior to skin removal by using tissue RNA-seq.
|
2 weeks prior to skin removal and 1 week prior to skin removal
|
|
To define the locations of the types of cells populating in the skin following fractionated laser resurfacing (FLR) wounding
Time Frame: 2 weeks prior to skin removal and 1 week prior to skin removal
|
Define the locations of the different cell types following FLR wounding at 2 weeks and 1 week prior to skin removal by using tissue RNA-seq.
|
2 weeks prior to skin removal and 1 week prior to skin removal
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jeffrey Travers, MD, PhD, Wright State University
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)
July 16, 2025
Primary Completion (Estimated)
December 1, 2028
Study Completion (Estimated)
December 1, 2028
Study Registration Dates
First Submitted
May 21, 2024
First Submitted That Met QC Criteria
June 28, 2024
First Posted (Actual)
July 5, 2024
Study Record Updates
Last Update Posted (Actual)
May 22, 2026
Last Update Submitted That Met QC Criteria
May 18, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023-312
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
Yes
product manufactured in and exported from the U.S.
Yes
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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