Skip to content

A Pharmacokinetic Study of Sevoflurane Inhalation in Burn ICU Patients

A Pharmacokinetic Study of Sevoflurane Inhalation in Burn ICU Patients

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02048683
Acronym
SEVOBURN
Enrollment
24
Registered
2014-01-29
Start date
2013-12-01
Completion date
2015-09-01
Last updated
2026-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ICU Patients With Indication of Sedation

Keywords

Pharmacokinetics, Sevoflurane, Burn, Sedation

Brief summary

Comparing a pharmacokinetic model of a short sevoflurane sedation in burn ICU patients with control ICU patients.

Detailed description

Prospective clinical study in ICU with sedated ventilated patients with sevoflurane with the AnaConda® system, establishing pharmacokinetic model of sevoflurane and its metabolites (hydroxyfluroisopropanol, fluoride) comparing burn and non burn ICU patients

Interventions

DRUGShort term sedation with sevoflurane in ICU

Sponsors

University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patients ventilated requiring invasive procedure in ICU * Stable respiratory and hemodynamic conditions * Consent of patients or family * Arterial line * Burn patients : burn area between 20 and 50% (3rd degree) OR non burn patients

Exclusion criteria

* BMI \<30 * Sevoflurane anaphylaxia

Design outcomes

Primary

MeasureTime frame
Determination of plasmatic concentrations of sevofluraneat 5min, 15 min, 60 min and just before the end of sedation.

Secondary

MeasureTime frame
Determination of plasmatic concentrations of HFIP and fluorideat 5min, 15 min, 60 min and just before the end of sedation. And 5min, 10 min, 30 min, 60 min and 120 min after the end of sedation

Countries

France

Contacts

PRINCIPAL_INVESTIGATORSébastien PERBET

University Hospital, Clermont-Ferrand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 8, 2026