Hypertension Clinical Trial
Official title:
A Pilot Study to Evaluate the Performance of Nihon Kohden's NTX Wireless Patient Monitoring System
Verified date | September 2012 |
Source | Vanderbilt University |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Observational |
- Determine the accuracy of the NTX wireless monitoring system alerts
- Evaluate patient compliance with wearing device
- Determine false alarm rates
Status | Completed |
Enrollment | 26 |
Est. completion date | June 2009 |
Est. primary completion date | January 2009 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - 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 Exclusion Criteria: - ICU patients - Female subjects who are pregnant - Patients < 18 years of age - Patients that have a contradiction for continuous Blood Pressure monitoring |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | Vanderbilt University Medical Center | Nashville | Tennessee |
Lead Sponsor | Collaborator |
---|---|
Vanderbilt University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Evaluation of patient compliance with wearing device | 24 hour minimum post op | No | |
Secondary | Determine accuracy of the NTX wireless monitoring system | duration of patient involvement | No | |
Secondary | Determine false alarm rates | duration of patient involvement | No |
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