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Effectiveness of Fractionated Laser Resurfacing to Protect Geriatric Skin From Actinic Neoplasia

Effectiveness of Fractionated Laser Resurfacing to Protect Geriatric Skin From Actinic Neoplasia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03906253
Enrollment
72
Registered
2019-04-08
Start date
2018-01-10
Completion date
2028-12-01
Last updated
2026-07-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Actinic Keratoses, Aging, Non-Melanoma Skin Cancer

Brief summary

This study is following up on previous studies that have demonstrated that geriatric subjects respond different to ultraviolet B (UVB) light than young subjects. The treatment of geriatric skin with dermal rejuvenation therapies (dermabrasion, fractionated laser resurfacing) restores the appropriate UVB response. Ongoing studies have tested the ability of fractionated laser resurfacing (FLR) to assess how long this wounding effect lasts-and have found that this appears to be a durable response which lasts for at least two years. The findings that FLR protects geriatric skin at two years is the impetus for this study. This study is an interventional study to assess if FLR treatment of one forearm of geriatric subjects with multiple actinic keratosis will result in the short-term removal of actinic keratosis, and the long-term decrease in levels of future actinic keratosis and other non-melanoma skin cancers in comparison to the untreated arm. Study length and visit: The first part of the study is completed in 1 day then there are follow up visits at 90 days and every 6 months for 5 years.

Interventions

A rejuvenating laser that makes tiny holes in the very superficial part of the skin.

Sponsors

Wright State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosed with Actinic Keratosis within the past 6 months * At least 60 years of age, or older * Ability to comprehend procedures and risks versus benefits * Able to provide Informed Consent * Fair Skin (Fitzpatrick Type I or II) * Possess both Right and Left Forearms

Exclusion criteria

* Uncontrolled Diabetes Mellitus * Not able to comprehend procedures or risks versus benefits * Pregnant or nursing * Large tattoos on forearms * History of abnormal healing or scarring (i.e., keloids) * Any disease that gets worse while in the sun * Use of topical or oral anti-inflammatory medication or steroids * Allergy to lidocaine * Current use of photosensitizing medication

Design outcomes

Primary

MeasureTime frameDescription
Change From Baseline in the Number of Actinic Keratosis due to FLR treatment.up to 5 yearsInvestigator will assess the number of actinic keratosis on both forearms.
Change From Baseline in the Number Non-Melanoma Skin Cancers due to FLR treatment.up to 5 yearsInvestigator will assess the number of actinic keratosis on both forearms.

Countries

United States

Contacts

CONTACTManager, Clinical Research Operations
pturesearch@wrightstatephysicians.org937-245-7500
CONTACTRegulatory Specialist
pturesearch@wrightstatephysicians.org937-245-7500
PRINCIPAL_INVESTIGATORJeffrey B Travers, MD, PhD

Wright State University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 18, 2026