Influence of Isoflurane inhalative sedation on the validation of liver function using liver maximum capacity (LiMAx®)-Test

• Conditions: K72.0; Acute and subacute hepatic failure

• Registration Number: DRKS00022228
• Lead Sponsor: niversitätsklinik für Anästhesiologie, operative Intensivmedizin, Rettungsmedizin, SchmerztherapieKlinikum Herford AöR

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-09-17
• Study Completion: 2020-12-21
• Results First Posted: 2024-04-08
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 22

Inclusion Criteria

Intensiv care patients sedatedwith Propofol/ Isoflurane.

Exclusion Criteria

Pregnancy

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Correlation of the LiMAx value measured during sedation with Propofol/Isoflurane with standard laboratory parameters related to liver function.

Secondary Outcome Measures

Name	Time	Method
Correlation of the LiMAx value measured during sedation with Propofol/Isoflurane with further standard laboratory parameters.