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Pharmacokinetic of Sevoflurane During a 48h Sedation in Intensive Care Unit With AnaConDa® (Anaconda)

U

University Hospital, Clermont-Ferrand

Status

Completed

Conditions

Sedation

Treatments

Other: sevoflurane

Study type

Interventional

Funder types

Other

Identifiers

NCT01196754
CHU-0079

Details and patient eligibility

About

This is a prospective clinical monocentric study in ICU with sedated ventilated patients with sevoflurane during 48 h with the AnaConda® system, establishing pharmacokinetic model of sevoflurane.

Full description

Prospective clinical monocentric study in ICU with sedated ventilated patients with sevoflurane during 48 h with the AnaConda® system, establishing pharmacokinetic model of sévoflurane and its metabolites (hydroxyfluroisopropanol, fluoride)

Enrollment

12 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients ventilated more than 48 h
  • Stable respiratory and hemodynamic conditions
  • Consent of patients or family
  • Arterial line

Exclusion criteria

  • Acute kidney injury
  • Obesity
  • Sevoflurane anaphylaxia

Trial design

12 participants in 1 patient group

sevoflurane
Other group
Treatment:
Other: sevoflurane

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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