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Performance of Two Different ke0s in the Same Pharmacokinetic Propofol Model

NCT01011192 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2009-11-13

No results posted yet for this study

Summary

The aim of this study was to assess the clinical performance of two different ke0s (fast and slow) in terms of propofol effect-site concentration (Ce) during the loss and recovery of consciousness, using Marsh's pharmacokinetic model.The hypothesis to be tested was that the Ce of propofol predicted by the slow ke0 in the loss and recovery of consciousness is similar, differently from the fast ke0.

Conditions

  • Unconsciousness

Sponsors & Collaborators

  • Hospital Santa Sofia Ltda

    collaborator UNKNOWN

  • Centro Medico Campinas

    lead OTHER

Principal Investigators

  • Ricardo F Simoni, MD · Centro Medico Campinas

Eligibility

Min Age
20 Years
Max Age
45 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-09-30
Primary Completion
2009-10-31
Completion
2009-11-30

Countries

  • Brazil

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01011192 on ClinicalTrials.gov