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Small study tests laser vs. punch biopsy for burn scars

NCT ID NCT03692273

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 whether laser treatment or a small punch biopsy (removing a tiny piece of scar tissue) improves burn scars better than no treatment. Seventeen adults with burn scars each had three small areas on one scar treated differently: laser, punch biopsy, or nothing. Researchers used photos, surveys, and tissue samples to see which approach worked best. The goal is to find better ways to improve scar appearance and quality of life for burn survivors.

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

17 people

The number who actually took part.

Started

Mar 2019

Finished

Oct 2025

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 years and older

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 must be 18 years of age or older * Must be medically fit to undergo laser/reconstructive procedure * Must have symptomatic HTBS for which they are already planning to undergo laser treatment. The symptomatic HTBSs may include the study scar area, but there must be other areas that the patient is getting treated with laser besides the study scar. * The HTBS must have occurred from a burn injured area either treated by skin grafts or allowed to heal secondarily. * Be willing and able to participate in the study with a year of follow-up * Must be able to answer surveys on their own, and not rely on surrogates * Not be pregnant or planning to become pregnant during the treatment phase of the study Study Scar Inclusion Criteria: * The study scar must be at least 3mm thick * For Extremities, no surgical treatment can be performed on joint space above or below the target area * If the study scar is over a joint, then no surgical treatments can occur to the body part above or below it * When the study scar is on the trunk or neck, it must not be on continuity or adjacent to any area of planned surgical treatment. * Study Scar Size: The study scar can either be within an area of homogenous HTBS or be an area of HTBS surrounded by normal tissue if it meets the following size criteria: * Within HTBS For treatment areas within burn scars, it must be 65cm2 or larger to permit 3 treatment areas that are 3 x 3cm with a 1cm wide segment of untreated scar between it. * Surrounded by normal tissue For treatment areas surrounded by normal skin, the treatment area must be 33cm2 or greater, contain similar 3x3cm treatment areas, and have intervening segments of 1cm of scar between treatment areas. A border around the scar, is not required here because it is surrounded by normal skin. Exclusion Criteria: * Previous laser or reconstructive procedures for the treatment of their HTBS in the study scar or adjacent tissue. * Steroids, immunosuppressive medications, chemotherapy or other medications that can delay their wound healing/immune function. * Medical Conditions that preclude laser treatment or general anesthesia if needed * Cognitively unable to complete PROMs on their own * The study area should not be part of a contracture or other hypertrophic scar that would be better treated with surgical procedures. * The study scar must not be adjacent to/in continuity with areas of HTBS that are planning to be treated with surgical interventions.

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Conditions

The condition(s) this trial relates to.

burn Cicatrix, Hypertrophic

As listed by the trial registrant

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

Contacts and locations

Locations

  • Massachusetts General Hospital

    Boston, Massachusetts, 02114, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.