Laser showdown: can a newer laser match the standard for HS?
NCT ID NCT06960447
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether alexandrite laser works as well as Nd:YAG laser for treating hidradenitis suppurativa (HS), a painful skin condition. Twenty-one people will receive both lasers on different sides of their body to compare results. The goal is to see if alexandrite can reduce symptoms and improve quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- laser treatment (Nd:YAG or alexandrite)
- What this could lead to
- If alexandrite laser works as well as Nd:YAG, it could give patients another effective option for easing HS symptoms.
- What could go wrong
- This is a small, early-stage study with only 21 participants, so results may not apply to everyone. Lasers can cause pain or skin reactions.
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
-
About 21 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Jul 2026
An estimate. Start dates often move.
- Expected to finish
-
Jul 2027
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
-
12 to 75 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 Hide 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: * Geisinger male or female patients with a diagnosis of hidradenitis suppurativa (all stages of disease) * 12-75 years of age * Not on concurrent systemic therapy (e.g., antibiotics, biologic therapies) * Must have not used systemic therapies within 2 weeks of enrollment in study * Able and willing to provide consent Exclusion Criteria: * Patients who cannot tolerate laser therapy * Patients who cannot wear protective eyewear * Patients who are pregnant
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Hidradenitis suppurativa (HS) are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- New pill aims to calm painful skin flares
- Can monthly selfies and symptom logs reveal how chronic skin diseases flare and settle?
- Can a Bladder-Derived patch improve wound healing in daily practice?
- Can a daily pill tame the painful lesions of hidradenitis suppurativa?
- Can a new injection quiet the painful lumps of hidradenitis suppurativa?
- Can a new injection tame the painful lumps of hidradenitis suppurativa?