Skip to main content
Clinical Trials/NCT00205517
NCT00205517
Terminated
Not Applicable

Pharmacokinetics and Dynamics in Patients Randomized to Once Daily Awakening and Sedated According to Standardized Algorithm

Virginia Commonwealth University0 sites75 target enrollmentSeptember 2002

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sedation
Sponsor
Virginia Commonwealth University
Enrollment
75
Primary Endpoint
Length of mechanical ventilation and ICU stay. Mortality
Status
Terminated
Last Updated
13 years ago

Overview

Brief Summary

Certain methods of sedation increase the duration of respiratory failure. Two strategies, a nursing- implemented sedation algorithm and daily interruption of sedatives, decrease length of mechanical ventilation compared to "conventional care" but have not been compared to each other. The reason certain methods of sedation lead to prolonged respiratory failure is unknown but may be related to altered pharmacokinetics and dynamics that are unique to critically ill patients. Critically ill patients receive substantial doses of sedatives over prolonged periods. The impact of these management strategies on short- and long-term psychiatric complications are unknown. The study seeks to test the central hypothesis that sedation practices impact strongly on outcome of respiratory failure and psychiatric complications. The three specific aims are (1) to compare two sedation strategies (protocol directed sedation and daily interruption of sedatives), (2) to examine the prevalence of psychiatric complications, and (3) to compute the pharmacokinetics of commonly used sedatives and narcotics.

These aims will be achieved by enrolling critically ill patients in a prospective randomized trial comparing the above mentioned sedation strategies, and assessing sedation level as well as delirium throughout the duration of respiratory failure. Sedative plasma levels will be measured, and pharmacokinetics computed. Psychiatric morbidity will be assessed by administration of validated questionnaires.

Registry
clinicaltrials.gov
Start Date
September 2002
End Date
July 2006
Last Updated
13 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients aged 18 and older undergoing mechanical ventilation via naso- or orotracheal tube -

Exclusion Criteria

  • Age less than 18, tracheotomy, severe dementia or mental retardation, severe neuromuscular disease or neuromuscular blockade use, institution of mechanical ventilation at another hospital

Outcomes

Primary Outcomes

Length of mechanical ventilation and ICU stay. Mortality

Secondary Outcomes

  • Physical and emotional well being. Length of time return to work. Morbidity assessed by questionnaire

Similar Trials