Accuracy Testing of Validated and Non-validated Home BP Devices Sold on the Online Market.
Recruiting · NCT06688409 · Interventional (participants receive a specific treatment) · Lead sponsor: Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal
View the official record on ClinicalTrials.gov →Interventions studied
awake ABPM
What this trial is about
This study aims to assess whether validated and non-validated blood pressure measuring devices sold on the online market are accurate in regards to the mean awake BP from ambulatory blood pressure monitoring.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Adults aged \> 18 years scheduled to undergo an ABPM
Exclusion criteria
- Upper arm size outside of cuff range of selected devices (\<22 cm or \>42 cm)
- Night shift workers
- Permanent atrial fibrillation
- Known severe aortic stenosis
- Contraindication to measure BP on the non-dominant arm
- Ongoing pregnancy
- Inability or unwillingness to provide consent
Where it is running
1 location listed.
- Hôpital Sacré-Coeur de Montréal - Montreal, Quebec, Canada