Status:
COMPLETED
Use of the PSA 4000 Monitor in the Post-Operative Period in Patients Undergoing Major Surgery
Lead Sponsor:
Mayo Clinic
Conditions:
Postoperative
Eligibility:
All Genders
18+ years
Brief Summary
Evaluate correlation between the values from the PSA monitor and clinical assessment of sedation with the RASS on postoperative patients.
Detailed Description
Assessing level of sedation in critically ill patients is an integral part of intensive care practice. Sedation scales, such as the Richmond Agitation-Sedation Score (RASS) 1, have been developed, but...
Eligibility Criteria
Inclusion
- Detailed Population Description: The study population will include those patients that have undergone surgery under general anesthesia at St. Marys Hospital, Mayo Clinic Rochester, admitted to the 7MB D/E Intensive Care Unit and require intubation and mechanical ventilation for a period of at least 4 hours after admission
Exclusion
Key Trial Info
Start Date :
July 1 2005
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
September 1 2008
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT00273169
Start Date
July 1 2005
End Date
September 1 2008
Last Update
January 15 2010
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Mayo Clinic
Rochester, Minnesota, United States, 55905