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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02860533
Other study ID # 2016-00871
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2016
Est. completion date February 1, 2017

Study information

Verified date May 2019
Source University Hospital, Basel, Switzerland
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The iPARR DELTA BP Study is designed to evaluate whether a new smartphone app using the photoplethysmography signal of the inbuilt camera can measure blood pressure (BP) fluctuations with sufficient correlation compared to the goldstandard oscillometric BP measurements. Investigators will recruit patients who are scheduled for a routine treadmill stress test and assess their blood pressure before and right after the test with the smartphone app and the standard BP measurements on the opposite upper extremity. Pronounced BP fluctuations are encountered during vigorous activities. The primary endpoint of the iPARR DELTA BP Study is the correlation of the absolute difference of subsequent measurements between both techniques. If the relative chances of BP fluctuations are sufficiently assessed with this new device, BP fluctuations could be monitored continuously after calibration.


Recruitment information / eligibility

Status Completed
Enrollment 220
Est. completion date February 1, 2017
Est. primary completion date February 1, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria:

- able to give informed consent

Exclusion Criteria:

- atrial fibrillation

- medical reasons why blood pressure measurement is not possible at the upper extremity (Shunt, Lymphedema)

Study Design


Related Conditions & MeSH terms


Intervention

Device:
cuff device
Measurement of blood pressure during stress testing with cuff device
iphone
Measurement of blood pressure during stress testing with iPhone

Locations

Country Name City State
Switzerland University Hospital Basel Basel BS

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Basel, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Absolute difference between conventional blood pressure measurements and the corresponding iPhone blood pressure estimations Difference between the delta of two sequential oscillometric measurements and the delta of the two corresponding blood pressure estimates calculated from the PPG signal of an iPhone 4S 1 day
Secondary Number of measurement failures Number of measurements that cannot be analyzed due to bad signal quality of the Photoplethysmography (PPG) signal 1 day
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