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At-Home light therapy could zap nail fungus

NCT ID NCT07012343

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 This study
Running, but no longer taking on new participants.
Completed
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tests a new home-use LED light device to treat nail fungus (onychomycosis). Researchers want to find the best light dose and how often to use it. Fifty adults with nail fungus will use the device at home and be monitored for improvement.

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

50 people

The number who actually took part.

Started

Jan 2025

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

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

Ages

18 to 70 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Patients diagnosed with onychomycosis (nail fungal infection) by a dermatologist. * Diagnosis criteria include at least one clinical criterion combined with at least one laboratory examination criterion. Clinical Criteria: * Discoloration patches/streaks on the nail. * Onycholysis (nail separation from the nail bed). * Subungual hyperkeratosis/debris (thickening under the nail). * Nail plate thickening. * Laboratory Examination Criteria: * Direct microscopy using KOH preparation. * Histopathological examination using Periodic Acid Schiff (PAS) stain. * Patients with distal lateral subungual onychomycosis (DLSO) of the fingernails or toenails, except for the little toenail. * Patients with onychomycosis who have limitations on or refuse oral antifungal treatment. * Individuals willing to participate in the research after receiving a full explanation of the research details, able to comply with the research procedures, and have signed the informed consent form. Exclusion Criteria: * Presence of nail abnormalities caused by other diseases or conditions. * Pregnant or breastfeeding. * History of receiving oral antifungal agents within the past 6 months or topical antifungal agents within the past 1 month prior to enrollment. * History of photosensitivity or photodermatitis. * Known allergy to methylene blue. * Presence of erythematous or oedematous inflammatory skin conditions near the site of onychomycosis. * Severe peripheral arterial disease. * Uncontrolled diabetes mellitus or HbA1C \> 8%. * Immunocompromised status, such as HIV infection with CD4 count \< 200 cells/mm³ or diagnosis of Acquired Immunodeficiency Syndrome (AIDS). * Current use of immunosuppressive medications, including Tacrolimus, Azathioprine, Cyclosporine, Mycophenolate mofetil, or Prednisolone \>10 mg/day.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Faculty of Medicine Chulalongkorn University

    Bangkok, Thailand