Timing of Surgery And Outcome in Burn Patients ( EARLYBURN ) (NCT02940171) | Clinical Trial Compass
TerminatedNot Applicable
Timing of Surgery And Outcome in Burn Patients ( EARLYBURN )
Stopped: Enrollment was stopped early due to heavy workload at burn care centers and the impact of the COVID-19 pandemic.
France470 participantsStarted 2016-12-25
Plain-language summary
The prognostic of burn patients has improved over the last decades. Early excision of full thickness burns is thought to be one of the key factors which have led to prognostic improvement. Best timing for burn excision remain uncertain, however. In this multicenter observational study, we aim at exploring the impact of timing of surgery on outcome in severely ill burn patients using a propensity analysis.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.