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Sponsors and Collaborators: |
Virginia Commonwealth University National Institutes of Health (NIH) American Lung Association |
Information provided by: | Virginia Commonwealth University |
ClinicalTrials.gov Identifier: | NCT00205517 |
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.
Condition | Intervention |
Sedation Mechanical Ventilation Depression Post-Traumatic Stress Disorder Quality of Life |
Procedure: Daily interruption of sedation versus sedation algorithm |
MedlinePlus related topics: | Critical Care Depression Post-Traumatic Stress Disorder Stress |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study |
Official Title: | Pharmacokinetics and Dynamics in Patients Randomized to Once Daily Awakening and Sedated According to Standardized Algorithm |
Estimated Enrollment: | 60 |
Study Start Date: | September 2002 |
Estimated Study Completion Date: | July 2006 |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
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
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Virginia Commonwealth University |
National Institutes of Health (NIH) |
American Lung Association |
Principal Investigator: | Marjolein de Wit, MD | Virginia Commonwealth University |
Study ID Numbers: | K23GM068842, K23GM068842 |
First Received: | September 12, 2005 |
Last Updated: | September 12, 2005 |
ClinicalTrials.gov Identifier: | NCT00205517 |
Health Authority: | United States: Federal Government |
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