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An 8-week study to investigate the benefits of a blue LED facial mask device on acne

An 8-week study to investigate the benefits of a blue LED facial mask device on acne

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14219895
Enrollment
30
Registered
2026-03-09
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-03-23

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

Conditions

Acne Skin and Connective Tissue Diseases

Interventions

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.

Sponsors

Lustre Skin Ltd
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 75 Years

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria

Exclusion criteria: 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

Countries

United Kingdom, Wales

Contacts

Public ContactStewart Long
stewart@cutest.co.uk+44 (0)2920 625686

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 3, 2026