Acne
Use of an LED mask daily for the study duration. Treatment is daily, every day for 8 weeks. Follow up is for 2 weeks post the final treatment.
1. Volunteers who are aged 14-75 years 2. Volunteers who have signed the consent form after the nature of the study has been fully explained 3. Volunteers who are able to provide signed informed consent (> 16 years) 4. Parents who are able to provide signed informed consent for those volunteers <16 years 5. Volunteers who have at least 5 blemishes at the time of consent 6. Volunteers who are willing to cooperate and participate by following study requirements
1. Pregnant, breastfeeding, or lactating females at the start of the study; those who have given birth in the past 6 weeks or those that planning to become pregnant during the study 2. Volunteers who have taken part in a Health Research Authority or MHRA regulated clinical trial (e.g., at a hospital or phase I unit) within the previous eight weeks 3. Volunteers who have taken part in a study involving the face within the previous 4 weeks 4. Volunteers with a recent history (previous 12 months) of significant skin disease requiring medical intervention, e.g., a dermatology outpatient appointment 5. Volunteers that have a history of facial skin cancer on the test areas 6. Volunteers with photosensitive disorders 7. Volunteers taking medications that can cause photosensitivity 8. Volunteers who have a medical history or seizures triggered by light 9. Volunteers with a recent exposure (previous four weeks) to the sun or sun beds, moderate to pronounced suntan, tattoos, scars or other disfigurement, significant dilated vessels, or other conditions on the test area that, in the opinion of the investigators, might influence the test results 10. Volunteers currently using topically applied prescription medications on/near the test site 11. Volunteers who have had chemical peels, dermabrasion or facial cosmetic surgery within the last 6 months