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Trial of a deep laser technique to prevent skin cancers in people with a strong history of them.

Trial of laser resurfacing to target mutation load in people with a strong history of skin cancers.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12618001513202
Enrollment
11
Registered
2018-09-10
Start date
2019-03-23
Completion date
2019-05-09
Last updated
2020-10-05

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

Conditions

None listed

Brief summary

The purpose of this study is to assess whether skin or wound repair using ‘ablative laser resurfacing’ assists in reducing sun-induced mutations and therefore reduces the number of non-melanoma skin cancers. Who is it for? You may be eligible for this study if you are over the age of 45 and have had more than 10 non-melanoma skin cancers in your life. Study details Consenting participants will have three 2.5 x 2.5cm patches of skin devoid of skin cancer identified on one forearm. Participants will then receive ablative laser resurfacing to two patches of skin. The third patch of skin will not receive any treatment This treatment will be performed at the Princess Alexandra Hospital. After 3 months, a biopsy of the three patches of skin and a saliva sample will be taken for assessment. It is hoped that this research will show that ablative laser resurfacing reduces the amount of skin mutations and thus may reduce the chance of skin cancer formation.

Interventions

Study participants aged 45 years or older with a history of more than 10 epidermal carcinomas will be considered. Patients will be excluded if they have used field therapy such as topical fluorouracil, photodynamic therapy, ingenol or imiquimod on the areas considered for treatment in the past 6 months; if they have had an organ transplantation or are on immunosuppressive therapy; if they have an active blood borne disease (e.g. HIV) or have a hereditary genetic condition favoring a skin cancer.

Study participants aged 45 years or older with a history of more than 10 epidermal carcinomas will be considered. Patients will be excluded if they have used field therapy such as topical fluorouracil, photodynamic therapy, ingenol or imiquimod on the areas considered for treatment in the past 6 months; if they have had an organ transplantation or are on immunosuppressive therapy; if they have an active blood borne disease (e.g. HIV) or have a hereditary genetic condition favoring a skin cancer. Dorsal forearms are used as they are often severely sun-exposed areas. ND-YAG ablative laser resurfacing will be conducted on the identified area under local anesthesia in the department of dermatology at the Princess Alexandra Hospital, Brisbane, by a dermatological surgeon. This method is preferred to dermabrasion as it is easier to control the depth and has a greater safety profile. Laser parameters include: wavelength of 2940nm, frequency of 8hz, 4-6 passes at different depths (equivalent to a depth of ablation 400 microns and 600 microns), overlap of 50%, dose is 25J/cm2 per pass. There is no cooling. In consenting patients and using a marker pen, three areas of skin, each measuring 25mm x 25mm (about the size of a ten cent piece) will be selected. These regions will not have any skin cancers on them. Two of these areas will be resurfaced and one will act as a control area. Two of the areas will then be injected with local anaesthetic. When the skin is numb both areas will be lasered, one to a depth of 0.4mm and the other to 0.6mm. This compares to the thickness of 1-2 business cards. This ‘resurfacing’ will remove the sun-damaged skin layers. The third area will not be treated and will be used as a control area. After 3 months, 2mm (diameter) biopsies will be taken from the resurfaced and the control areas. A saliva specimen will be used for reference genomic DNA. Whole exome sequencing will be conducted at 500X depth.

Sponsors

University of Queensland Diamantina Institute
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Other
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
45 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Participants must: have had more than 10 skin cancers such as BCC (basal cell carcinoma) or SCC (squamous cell carcinoma).

Exclusion criteria

*having had forearms treated with topical fluorouracil (e.g.Efudix) or photodynamic therapy or ingenol (Picato) or imiquimod (Aldara) in the last 6 months *having had an organ transplantation or be on immunosuppressive therapy *having any active blood borne diseases (e.g. HIV, HBV, HCV) *having a hereditary genetic condition favoring a skin cancer

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026