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

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

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Key information

Conditions

Blood Pressure

Age range

25 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Basel

Basel, Canton of Basel-City, 4051, Switzerland

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

Somnotouch NIBP

Device

Somnotouch NIBP in addition to standard blood pressure measurement

Primary outcomes

Difference in mean 24h systolic blood pressure

Time frame: 24 hours

Difference in mean 24h systolic blood pressure

Sponsors and collaborators

Lead sponsor

University Hospital, Basel, Switzerland

Other

Registry information

Acronym: VAST

Important dates

Study start: 2017
Primary completion: 2018
Study completion: 2018
First posted: Feb 15, 2017
Registry last updated: Jun 15, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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Completed