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Clinical Trials/KCT0001760
KCT0001760
Recruiting
未知

Population pharmacokinetic and pharmacodynamic modeling of propofol in underweight patients under general anesthesia

Asan Medical Center0 sites20 target enrollmentTBD
ConditionsNot Applicable

Overview

Phase
未知
Intervention
Not specified
Conditions
Not Applicable
Sponsor
Asan Medical Center
Enrollment
20
Status
Recruiting
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. 20 yr \< age \<65 yr
  • 2\. BMI (body mass index) \< 18\.5 (kg/m2\)
  • 3\. Hemoglobin \> 9 g/dl
  • 4\. Patients who signed a written informed consent form

Exclusion Criteria

  • 1\-1\. Patients with severely impaired respiratory function or respiratory depression status
  • 1\-2\. Patients with convulsive disorders, head injury, shock, a reduced level of consciousness of uncertain origin, intracranial lesions or increased intracranial pressure, or in patients with severe hepatic impairment
  • 1\-3\. Patients who are concurrently taking other CNS depressants that may cause respiratory depression, hypotension, profound sedation or potentially result in coma
  • 1\-4\. Clinically significant impairment of cardiovascular, respiratory and renal function
  • 2\. Patients with known hypersensitivity to intervention treatments (propofol) or to any of the excipients
  • 3\. Patients who are considered by the investigator to be unsuitable to participate in the study for any other reason not mentioned in the inclusion and exclusion criteria.

Outcomes

Primary Outcomes

Not specified

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