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

No results posted yet for this study

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

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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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00273169 on ClinicalTrials.gov