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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03271268
Other study ID # StLouisFrance
Secondary ID
Status Recruiting
Phase N/A
First received August 31, 2017
Last updated September 4, 2017
Start date August 6, 2017
Est. completion date April 6, 2019

Study information

Verified date September 2017
Source Saint-Louis Hospital, Paris, France
Contact Sabri Soussi, MD
Phone 0613064542
Email sabri.soussi@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Burn injury leads to hypovolemic then distributive shock. Fluid resuscitation remains the cornerstone of initial treatment of burn shock. However, fluid rescucitation can lead to fluid overload, which manifests most notably as lung edema.

The peptide NT-pro-BNP, a biomarker of cardiac congestion secreted by the myocardium, as well as plasma CD146, an endothelial factor involved in angiogenesis and a marker of vascular congestion, may help identifying patients with risk of pulmonary edema and hypoxia .

Our hypothesis is that these biomarkers may predict the occurence of pulmonary edema in severe burns patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 36
Est. completion date April 6, 2019
Est. primary completion date February 6, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Intubated mechanically-ventilated patients within the first 24 hours of admission

- And/or patients with total body surface area (TBSA) burn-injured >20 %

- And/or patients with at least 10% full-thickness burns

- And/or receiving vasopressors within the first 24 hours of admission

- And monitored by a PiCCO system (PiCCO-2 Pulsion Medical Systems AG, Munich, Germany)

Exclusion Criteria:

- Admission delay to ICU > 24 hours post burn

- Age less than 18 years

- Pregnancy

- Chronic renal impairment with a baseline eGFR < 15 ml/min

- Patients with chemical or electrical burns

- Coexisting non-burn trauma

- Patients moribund on admission or dead within 72 h from admission

- Patients with do-not-resuscitate orders

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Sabri SOUSSI Paris Ile de France

Sponsors (1)

Lead Sponsor Collaborator
Saint-Louis Hospital, Paris, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Lung edema Extravascular lung water (EVLW) > 10 mL/Kg as measured by transpulmonary thermodilution (TPTD) During the first 7 days of admission
Secondary Hypoxemia PaO2/FiO2 ratio of <200 During the first 7 days of admission for mechanically-ventilated patients
Secondary Hypercapnia PaCO2> 45 mmHg During the first 7 days of admission for mechanically-ventilated patients
Secondary Corrected minute ventilation > 10L/min Minute ventilation Ă— partial [Paco2]/40) > 10L/min During the first 7 days of admission for mechanically-ventilated patients
Secondary Multiple organ dysfunction syndrome (MODS) Sequential Organ Failure Assessment score (SOFA) = 8 During the first 7 days of admission
Secondary 28-day mortality 28 days
Secondary 90-day mortality 90 days
Secondary Length of stay in the ICU until 90 days of hospitalization
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