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NCT03054688 Clinical Trial

Somnotouch-NIBP Compared to Standard Ambulatory 24 Hours Blood Pressure Measurement

Blood Pressure Clinical Trial

— VAST  

Official title:
Somnotouch-NIBP Compared to Standard Ambulatory 24 Hours Blood Pressure Measurement

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03054688
Other study ID # 03061989
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 25, 2017
Est. completion date April 1, 2018

Study information
Verified date June 2018
Source University Hospital, Basel, Switzerland
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparison of 24 hours blood pressure measurement with puls-transit time versus cuffs.

Recruitment information / eligibility
Status Completed
Enrollment 83
Est. completion date April 1, 2018
Est. primary completion date March 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years and older
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:
• Somnotouch NIBP
Somnotouch NIBP in addition to standard blood pressure measurement

Locations
Country Name City State
Switzerland University Hospital Basel Basel Basel City

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 Difference in mean 24h systolic blood pressure Difference in mean 24h systolic blood pressure 24 hours
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