Somnotouch-NIBP Compared to Standard Ambulatory 24-hours Blood Pressure Measurement
Completed
- Conditions
- Blood Pressure
- Registration Number
- NCT03975582
- Lead Sponsor
- University Hospital, Basel, Switzerland
- Brief Summary
Comparison of 24 hours blood pressure measurement with puls-transit time versus cuffs.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 115
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
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Difference in mean 24 hours systolic blood pressure 24 hours Difference in mean 24 hours systolic blood pressure
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What are the molecular mechanisms underlying puls-transit time blood pressure measurement in Somnotouch-NIBP?
How does Somnotouch-NIBP compare to standard ambulatory blood pressure monitoring in terms of accuracy and patient compliance?
Are there specific biomarkers that correlate with improved outcomes using puls-transit time technology for hypertension management?
What adverse events are associated with cuffless blood pressure monitoring devices like Somnotouch-NIBP in long-term use?
How might Somnotouch-NIBP influence the adoption of non-invasive blood pressure monitoring in cardiovascular disease management?
Trial Locations
- Locations (1)
University Hospital Basel
🇨🇭Basel, Basel Stadt, Switzerland
University Hospital Basel🇨🇭Basel, Basel Stadt, Switzerland