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Clinical Trials/NL-OMON34762
NL-OMON34762CompletedNot Applicable

Modeling the respiratory effects of subanesthetic doses of propofol under closed-loop or non-steady-state conditions without and with a remifentanil background infusion in healthy volunteers. - Modeling the respiratory effects of a propofol-remifentanil interaction

eids Universitair Medisch Centrum0 sites24 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
24

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 to 99 (—)

Inclusion Criteria

  • Healthy volunteers of either sex in age range 18-45 years.

Exclusion Criteria

  • Obesity (BMI > 35)
  • Presence of medical disease
  • Presence of psychiatric disease
  • History of chronic alcohol or illicit drug use
  • Allergy to study medications
  • Difficult to hold to subject on mask causing leakage and inability to perform mask ventilation (i.e. Mallampati classification 3 or greater)
  • For females we require use of contraceptives

Investigators

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