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Timing of burn surgery: early or late? study ends early without clear answer

NCT ID NCT02940171

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
The trial has finished. Results may not be published yet.
Stopped early This study
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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study aimed to find out whether performing surgery within 48 hours of a severe burn (early excision) or later improves survival. It planned to follow 470 severely burned adults, but was terminated early and did not complete enrollment. Because of this, the results are limited and cannot provide a clear answer on the best timing for surgery.

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 clear results were obtained, this could help doctors decide the best time to operate on severe burn patients to improve survival.
What could go wrong
The study was terminated early, so it did not collect enough data to draw reliable conclusions. The findings may not apply to all burn patients.

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.

Participants

470 people

The number who actually took part.

Started

Dec 2016

Finished

Dec 2023

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.

Who is studied

Patients with extensive skin burns, defined as greater than 20% of the total body surface

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: * Age \>18 years * Admission to a burn unit within 72 hours from a burn injury * Total burned surface area (TBSA)\>20%(2nd degree or 3rd degree) for any type of burn * Patient covered by the social security * Non-opposition to participate to the study and to the constitution of the biological collection Exclusion Criteria: * Decline to participate * Decision not to resuscitate order before surgery * Pregnant or breastfeeding patiente * Decision to limit therapies in the first 24 hours * Patient not resident in France * Patient deprived of liberty

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Conditions

The condition(s) this trial relates to.

burn Critical Illness

As listed by the trial registrant

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

Contacts and locations

Locations

  • Departement of Anesthesiology, Critical Care and Burn Unit; Saint-Louis hospital, University Paris Diderot

    Paris, 75010, France

More trials for these conditions

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