Use of the PSA 4000 Monitor in the Post-Operative Period in Patients Undergoing Major Surgery
Completed
Conditions studied: Postoperative
In brief
Evaluate correlation between the values from the PSA monitor and clinical assessment of sedation with the RASS on postoperative patients.
Key facts
- Study ID
- NCT00273169
- Run by
- Mayo Clinic
- People needed
- 50
- Starts
- 2005-07-01
- Expected to finish
- 2008-09-01
- Last updated by the study team
- 2010-01-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Mayo Clinic — Rochester, Minnesota, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.