Validation of the NTX Wireless Patient Monitoring System

Completed

Conditions studied: Desaturation, Bradycardia, Tachycardia, Hypertension, Hypotension

In brief

* Reduction in time to detection of Clinically Significant events * Reduction of time to Intervention during Clinically Significant events * Reduction in the number of admissions to Intensive Care

Key facts

Study ID

NCT00644644

Run by

Vanderbilt University Medical Center

People needed

1303

Starts

2008-03-01

Expected to finish

2010-01-01

Last updated by the study team

2017-04-11

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Ability to give written informed consent
• Patients that are hospitalized for longer than 24 hours and are located on the 4th, 5th, or 6th floor of the Vanderbilt University Medical Center Round Wing
• Patients must be ≥18 years of age

You may not qualify if…

• ICU patients
• Female subjects who are pregnant
• Patients < 18 years of age
• Patients that have a contradiction for continuous Blood Pressure monitoring

Where it is running

• Vanderbilt University Medical Center — Nashville, Tennessee, 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.