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Sponsored by: |
Vanderbilt University |
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Information provided by: | Vanderbilt University |
ClinicalTrials.gov Identifier: | NCT00654693 |
Condition | Intervention |
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Desaturation Bradycardia Tachycardia Hypertension Hypotension |
Other: Rapid Response Team |
Study Type: | Observational |
Study Design: | Cohort, Prospective |
Official Title: | A Pilot Study to Evaluate the Performance of Nihon Kohden's NTX Wireless Patient Monitoring System |
Estimated Enrollment: | 150 |
Study Start Date: | March 2008 |
Estimated Study Completion Date: | June 2009 |
Estimated Primary Completion Date: | January 2009 (Final data collection date for primary outcome measure) |
Groups/Cohorts | Assigned Interventions |
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monitored
patients hospitalized for longer than 24 hours and are located on the 4th, 5th, and 6th floors of the Vanderbilt University Medical Center Round Wing
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Other: Rapid Response Team
If the subject is experiencing a life threatening change in their vital signs, the Rapid Response Team will be initiated per VUMC protocol.
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Approximately 150 patients will have wireless monitors attached to their arm. They will have their vital signs filtered through software that generates alerts and records data. The alert engine will produce pager and application based pop-up alerts which will be sent to the research nurse. Low and high limit alarms will be set according to the published guidelines (Hillman, K. et. Al., Resuscitation 48(2): 105-10, 2001) and adjusted at will by the response team.
During this portion of the study, the following research related procedures will be performed:
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Participants will be recruited in the Vanderbilt University Medical Center pre-operative clinic or in the Round Wing, after the effects of anesthesia have worn off. Before performing any trial-related procedures, written Informed Consent and HIPAA authorization will be obtained.
Inclusion Criteria:
Exclusion Criteria:
United States, Tennessee | |
Vanderbilt University Medical Center | |
Nashville, Tennessee, United States, 37212 |
Principal Investigator: | James M Berry, M.D. | Vanderbilt University |
Responsible Party: | Vanderbilt University ( James M. Berry, M.D. ) |
Study ID Numbers: | 080021 |
Study First Received: | April 3, 2008 |
Last Updated: | April 3, 2008 |
ClinicalTrials.gov Identifier: | NCT00654693 |
Health Authority: | United States: Institutional Review Board |
NTX Nihon Kohden mobile monitoring monitoring nihon |
kohden monitoring device remote monitoring wireless |
Hypotension Heart Diseases Tachycardia Bradycardia |
Vascular Diseases Arrhythmias, Cardiac Hypertension |
Pathologic Processes Cardiovascular Diseases |