The study of the effects of intellectual disability and oral antiepileptic drugs on awaking from general anesthesia

Not Applicable

Suspended

• Conditions: Dental patients undergoing total intravenous anesthesia

• Registration Number: JPRN-UMIN000039855
• Lead Sponsor: Okayama University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-04-01
• Study Completion: 2023-03-31
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Suspended
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Not provided

Exclusion Criteria

1)Patients with contraindications for propofol, remifentanil, rocuronium, 2)Patients who are judged to be inappropriate for study participation

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1)Blood concentration of propofol at the discontinuation of propofol and tracheal extubation, 2)Time from the discontinuation of propofol to tracheal extubation and 3)BIS value at tracheal extubation

Secondary Outcome Measures

Name	Time	Method
1)Propofol amount and average infusion rate of propofol, 2)Estimated blood concentration of propofol at the discontinuation of propofol and tracheal extubation, 3)Remifentanil amount and average infusion rate of remifentanil, 4)BIS values before & during anesthesia, and at the discontinuation of propofol.