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Glow at home: LED mask may fight wrinkles and sun damage

NCT ID NCT07025837

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested a light-emitting diode (LED) face and neck mask in 38 women aged 25–55 with signs of skin aging and sun damage. Participants used the mask daily for 10 minutes over 12 weeks. Researchers checked photos and surveys to see if the mask improved wrinkles, pigmentation, redness, and overall skin health.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
LED light therapy device
What this could lead to
If it works, this could offer a simple at-home option to reduce fine lines, wrinkles, and sun damage without creams or procedures.
What could go wrong
This was a small, short study with no placebo group, so results may not be reliable. Improvements could be minor or due to natural changes over time.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

38 people

The number who actually took part.

Started

Oct 2024

Finished

Feb 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

25 to 55 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Female * Aged 25-55 years. * Willing to follow the study protocols. * Self-reported issues with at least two of the following: Fine lines, Wrinkles, Hyperpigmentation, Dark spots, Reduced elasticity * Self-report concerns with at least one of the following: Crepey skin on the neck and chest, Sun damage on neck and chest * Willing to avoid introducing any new products, prescription medications, or supplements that target skin health during the study period. * If taking oral supplements or herbal remedies targeted at skin health and appearance, have been consistently taking these for at least 3 months prior to starting the study. * Is willing to maintain the routine of any oral supplements or herbal remedies targeted at skin health and appearance for the duration of the study. * Has been using the same skincare routine for at least one month prior to the study start date. * Willing to maintain the same skincare routine and products throughout the study. * Willing to avoid direct sun exposure during the study duration * Willing to wear sunscreen if have to be in the sun Exclusion Criteria: * Anyone who is extremely satisfied with their skin. * Anyone who has any chronic health conditions such as oncological (cancer) or psychiatric disorders. * Anyone who is planning to undergo facial treatments during the study period, including botox, dermal filler, chemical peels, etc. or has experienced any of these treatments in the last 3 months. * Anyone diagnosed with a skin condition affecting the face and/or neck who has had an active flare-up or breakout within the last year. This includes but is not limited to acne, eczema, psoriasis, rosacea, seborrheic dermatitis, vitiligo, urticaria (hives), warts, atopic dermatitis, melasma, and contact dermatitis. * Currently using any prescription medications that may affect the skin condition including but not limited to the following: * Corticosteroids like prednisone, methylprednisolone * Antipsychotics like olanzapine (Zyprexa), risperidone (Risperdal), quetiapine (Seroquel) * SSRIs and SNRIs like fluoxetine (Prozac), sertraline (Zoloft), venlafaxine (Effexor) * Anticonvulsants like phenytoin (Dilantin), lamotrigine (Lamictal), and carbamazepine (Tegretol) * Antihypertensives like lisinopril (Zestril), amlodipine (Norvasc), and propranolol (Inderal) * Antithyroid medications like Tapazole (methimazole), Propyl-Thyracil (propylthiouracil) * Anyone with a history of skin cancer or precancerous skin lesions on the face. * Anyone who has any known serious allergic reactions that require the use of an Epi-Pen. * Anyone who has any known allergies to ingredients commonly found in skincare products. * Anyone who is pregnant, breastfeeding, or trying to conceive * Anyone who cannot/will not commit to the study protocol. * Anyone with a history of substance abuse. * Anyone who has undergone an invasive medical procedure in the three weeks prior to the study or has a procedure planned during the study duration. * Anyone with a known allergic reaction to aluminum or plastics. * Anyone who suffers from any photosensitive disorder (sensitization to light). * Anyone with uncontrolled acne. * Anyone taking any prescription medication, over-the-counter supplements, or herbal supplements regularly (three or more days per week) that can cause photosensitivity including but not limited to the following: * Antibiotics like tetracyclines (e.g., doxycycline, tetracycline) or sulfonamides (e.g., Bactrim), fluoroquinolones (e.g., ciprofloxacin, levofloxacin) * Antifungals like Griseofulvin or Vfend (voriconazole) * Diuretics like drugs ending in -thiazides * NSAIDs like ibuprofen and Aleve (naproxen) * Retinoids or Vitamin A (e.g., Accutane (isotretinoin), (Retin-A) tretinoin * Antidepressants (e.g., SSRIs, Elavil (amitriptyline), Tofranil (imipramine) * Antihistamines like Phenergan (promethazine) * Antimalarial medications * Statins like Lipitor (atorvastatin), Zocor (simvastatin) * Antiarrhythmics like Pacerone (amiodarone) * St. John's wort * Anyone who suffers from light-induced headaches or migraines. * Anyone with a medical history of seizures or epilepsy triggered by light. * Anyone with an electronic implanted device such as a defibrillator, neurostimulator, pacemaker, or ECG monitor. * Anyone with a known history of carotid artery disease, stroke or transient ischemic attack (TIA), carotid stenosis, unstable blood pressure, easy fainting, thyroid disease, or of individuals about to undergo surgical procedures in the neck area. * Anyone who has stopped hormonal birth control in the past month.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Citruslabs

    Las Vegas, Nevada, 89118, United States

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