Optimal End-Tidal Sevoflurane concentration in patients with shock undergoing general anesthesia

Completed

• Conditions: Patients with shock; Patient with shock; Sevoflurane; MAC of sevoflurane; End tidal of sevoflurane

• Registration Number: TCTR20240321004
• Lead Sponsor: KhonKaen university

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2023-08-12
• Study Start: 2024-03-21
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 15

Inclusion Criteria

1. Aged 18 to 65 years old
2. Patients with shock undergoing general anesthesia

Exclusion Criteria

1. Decline to participate in the study
2. Pregnancy
3. History of seizures
4. History of Malignant hyperthermia
5. History of regular alcohol consumption
6. Patients with neurological conditions
7. End-stage kidney or liver disease
8. Who are unable to apply bispectral index monitor

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
sevoflurane concentration Intraoperation End tidal and Minimum alveolar concentrations

Secondary Outcome Measures

Name	Time	Method
Minimum alveolar concentration of seoflurane in patients with shock Intraoperation MAC