- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03265678
Skin Ageing Signatures and Cancer (SASAC)
Identification of a Genomic/Transcriptomic Signature for Ageing and Predisposition to Skin Cancer in Normal Sun-exposed Skin
The aim of this study is to identify genetic patterns in normal ageing skin in order to better understand age-related changes.
Data has suggested that skin ageing has a genetic basis and past studies have identified genes that promote skin aging due to sun exposure.
Study Overview
Status
Conditions
Detailed Description
This study will use new tools in an attempt to understand the small changes that take place in skin and may be linked to skin ageing either due to age or the effect of the sun. Some data suggests that these changes may have a genetic basis.
In this study, the doctor will use a clinical scale to assess the participants skin type, the scale will range from 1-5 with 1 being fairer skin types and 5 being darker skin types. The doctors will select 10 female participants who meet the required skin types (1-4), aged between 55 and 65 years who attend clinics for reasons other than skin cancer or other skin diseases. 5 of these patients will have high levels of skin ageing and 5 will have low levels of skin ageing as defined by a set of pre-defined criteria. The criteria will be identified by examining the skin on the participants face and forearm. The study sponsor will collect skin and blood samples from all participants in the high and low skin ageing groups and these will be sent to a specialist laboratory for DNA and RNA analysis (genetic analysis).
The study sponsor hope that this will help us understand the effects of ageing on skin's normal functions but also help us interpret results coming out of other genetic studies in skin cancer. This information will help to better understand the changes linked with the development of skin cancer.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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London, United Kingdom, E1 1BB
- Barts Health NHS Trust
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Able to give written informed consent prior to admission to this study.
- Female aged between 55 and 65 years.
- Willing and able to comply with clinical/photographic assessment and laboratory tests
Exclusion Criteria:
- Previous history of skin cancer, active inflammatory or other skin condition that in the opinion of the investigator may affect the skin ageing assessment.
- Feverish symptoms which lasted for ≥48 hours prior to study entry.
- Currently suffering from or having suffered during the last month, with any common systemic disease except arterial hypertension.
- Received any of the following treatment for more than 6 months during the last two years: hypo or hyperthyroidism treatment, corticoids, non-steroids anti-inflammatory, antihistamines, immunosuppressive treatments, diuretics, antibiotics, anticoagulants, beta blockers.
- Currently experiencing or having experienced in the last two months prior to study entry problems affecting the skin of the face or forearm for instance acne, eczema, psoriasis, seborroheic dermatitis, herpes zoster.
- Currently receiving or having received in the last two months prior to study entry any of the following dermatological treatments for more than 8 days: hormone based cream, retinoid based facial cream, > 8% concentration alpha hydroxy acid based cream, topical steroids, antibiotics and antifungals
- Previous facial aesthetic treatments such as: lifting, chemical peeling, dermabrasion, electrocoagulation, laser, sclerotherapy, reconstructive surgery, botox injection, filler injection.
- Currently using a hormone based cream that is applied on the forearm for hormonal replacement therapy.
- Have had a change in skin colour during within one month prior to study entry due to sun exposure
- Had a session of UV therapy for treatment purposes or in a beauty salon within one month prior to study entry.
- Use of a self-tanning product
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Arm
Registered participants will undergo a clinical assessment to determine whether they have high or low levels of skin ageing.
The study will recruit 5 subjects with low levels of skin ageing and 5 subjects with high levels of skin ageing.
Recruited patients will undergo skin punch biopsies, blood sampling and collection of lifestyle data.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Recruitment of 10 patients with high or low skin ageing scores and collection of normal sun exposed and non-sun exposed skin and blood for genetic analysis.
Time Frame: 1 Year
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Identify a genomic/transcriptomic molecular signature for skin ageing by correlation of whole genome sequencing and transcriptomic profiles of normal skin and clinically evaluated skin ageing scores
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1 Year
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Whole genome sequencing and transcriptomic analysis of normal skin samples
Time Frame: 1 Year
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Comparison of genomic and transcriptomic molecular signature for skin ageing with known genomic and transcriptomic signatures for cSCC
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1 Year
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Prof Catherine Harwood, Queen Mary University of London
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 11701
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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