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Stitches or not? study tests best way to heal after a skin biopsy

NCT ID NCT04623372

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 01, 2026 · Last updated Jul 02, 2026 · Updated 1 time

Summary

This study compares two ways of caring for a small skin biopsy wound: stitching it closed or letting it heal naturally with just a bandage. About 290 adults having a 4mm punch biopsy will be randomly assigned to one method. Doctors and patients will rate the scar's appearance and report pain during healing to see which approach works better.

What this could mean

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

What this could lead to
If one method proves clearly better, it could simplify healing instructions and improve scar outcomes for millions of skin biopsies each year.
What could go wrong
This is a small, single-center study comparing two common procedures, so results may not apply to all skin types or biopsy sizes. The outcome is based on subjective scar ratings.

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

290 people

The number who actually took part.

Started

Feb 2021

Finished

Dec 2024

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: * adult person (age greater than or equal to 18 years) * either hospitalized patient in a conventional or in a day care department, either seen at a medical appointment in Le Mans General Hospital * person on whom the indication of one or several skin biopsy(ies) using a punch of 4 mm diameter has been established * affiliated or beneficiary of a statutory social insurance scheme * free and informed written consent, signed by both the participant and the investigator (the day of inclusion at the latest and prior to any examination needed by the protocol) after an oral and written information Exclusion Criteria: * skin biopsy on the face or the cervical area * pregnant, breastfeeding or parturient woman * person deprived of liberty by an administrative act or a court decision * patient requiring compulsory mental health care * minor or legally protected adult * patient that is no longer in a condition to express his or her wishes * person that have participated or that are taking part in an interventional study over the past 30 days (condition of exclusivity)

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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

  • Centre Hospitalier Du Mans

    Le Mans, 72000, France