Use of the PSA 4000 Monitor in the Post-Operative Period in Patients Undergoing Major Surgery
NCT00273169 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50
Last updated 2010-01-15
Summary
Evaluate correlation between the values from the PSA monitor and clinical assessment of sedation with the RASS on postoperative patients.
Conditions
- Postoperative
Sponsors & Collaborators
- lead OTHER
Principal Investigators
-
Francis X. Whalen, Jr., M.D. · Mayo Clinic
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-07-31
- Primary Completion
- 2008-09-30
- Completion
- 2008-09-30
Countries
- United States
Study Locations
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