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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT03975582
Recruitment Status : Recruiting
First Posted : June 5, 2019
Last Update Posted : July 9, 2019
Information provided by (Responsible Party):
University Hospital, Basel, Switzerland

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

Condition or disease
Blood Pressure

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Study Type : Observational
Estimated Enrollment : 300 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Somnotouch-NIBP Compared to Standard Ambulatory 24 Hours Blood Pressure Measurement - a Prospective Registry
Actual Study Start Date : July 4, 2019
Estimated Primary Completion Date : June 2022
Estimated Study Completion Date : June 2022

Primary Outcome Measures :
  1. Difference in mean 24 hours systolic blood pressure [ Time Frame: 24 hours ]
    Difference in mean 24 hours systolic blood pressure

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
All patients from the medical outpatient clinic of the University Hospital of Basel with an indication for an ambulatory 24h blood pressure measurement.

Inclusion Criteria:

  • Age ≥ 18 years
  • Ability to give informed consent

Exclusion Criteria:

  • Age < 18 years
  • Medical reasons that forbid blood pressure measurements on upper extremities
  • Not able to give informed consent

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT03975582

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Contact: Thilo Burkard, MD 0041 61 265 25 25
Contact: Philipp Krisai, MD 0041 61 265 25 25

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University Hospital Basel Recruiting
Basel, Basel Stadt, Switzerland, 4031
Contact: Thilo Burkard, MD    061 2656565   
Sponsors and Collaborators
University Hospital, Basel, Switzerland
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Principal Investigator: Thilo Burkard, MD University Hospital, Basel, Switzerland

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Responsible Party: University Hospital, Basel, Switzerland Identifier: NCT03975582     History of Changes
Other Study ID Numbers: VAST-Registry
First Posted: June 5, 2019    Key Record Dates
Last Update Posted: July 9, 2019
Last Verified: July 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No