Clinical Trials Directory

Trials / Completed

CompletedNCT02940171

Timing of Surgery And Outcome in Burn Patients ( EARLYBURN )

Impact of Timing of Surgery on Outcome of Severely Ill Burn Patients

Status
Completed
Phase
Study type
Observational
Enrollment
470 (actual)
Sponsor
Assistance Publique - Hôpitaux de Paris · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed description

The first aim of the study is to explore the impact of timing of the first surgery on outcome of severely ill burn patients. Because a randomization would not be feasible in this setting, we will use a propensity analysis in matching patients receiving early surgery and those receiving late surgery. Secondary aims are to evaluate the impact of the timing of surgery on morbidity (organs failure, infections, sepsis) but also to assess the diagnostic and prognostic value of plasma and urine biomarkers in severely ill burn patients

Conditions

Interventions

TypeNameDescription
PROCEDUREEarly Excision of full thickness burnfirst excision surgery of full -thickness burn performed within 48 hours from burn injury
PROCEDURELate Excision of full thickness burnfirst excision surgery of full -thickness burn performed after 48 hours from burn injury

Timeline

Start date
2016-12-25
Primary completion
2023-12-11
Completion
2023-12-11
First posted
2016-10-20
Last updated
2024-07-10

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02940171. Inclusion in this directory is not an endorsement.