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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03265678
Other study ID # 11701
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2, 2017
Est. completion date January 22, 2018

Study information

Verified date April 2024
Source Queen Mary University of London
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date January 22, 2018
Est. primary completion date January 22, 2018
Accepts healthy volunteers
Gender Female
Age group 55 Years to 65 Years
Eligibility Inclusion Criteria: 1. Able to give written informed consent prior to admission to this study. 2. Female aged between 55 and 65 years. 3. Willing and able to comply with clinical/photographic assessment and laboratory tests Exclusion Criteria: 1. Previous history of skin cancer, active inflammatory or other skin condition that in the opinion of the investigator may affect the skin ageing assessment. 2. Feverish symptoms which lasted for =48 hours prior to study entry. 3. Currently suffering from or having suffered during the last month, with any common systemic disease except arterial hypertension. 4. 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. 5. 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. 6. 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 7. Previous facial aesthetic treatments such as: lifting, chemical peeling, dermabrasion, electrocoagulation, laser, sclerotherapy, reconstructive surgery, botox injection, filler injection. 8. Currently using a hormone based cream that is applied on the forearm for hormonal replacement therapy. 9. Have had a change in skin colour during within one month prior to study entry due to sun exposure 10. Had a session of UV therapy for treatment purposes or in a beauty salon within one month prior to study entry. 11. Use of a self-tanning product

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United Kingdom Barts Health NHS Trust London

Sponsors (2)

Lead Sponsor Collaborator
Queen Mary University of London University of Edinburgh

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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. 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 1 Year
Secondary Whole genome sequencing and transcriptomic analysis of normal skin samples Comparison of genomic and transcriptomic molecular signature for skin ageing with known genomic and transcriptomic signatures for cSCC 1 Year
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