A Multi-centre Study To Evaluate the auto-cuff Response During home vs Ambulatory bp Monitoring

A Multi-centre Study To Evaluate the auto-cuff Response During home vs Ambulatory bp Monitoring - AMSTERDAM

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON37664

Enrollment

450

Registered

2012-07-30

Start date

2012-10-11

Completion date

Unknown

Last updated

2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

elevated blood pressure Hypertension

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Reffered to Home Blood Pressure Measurement or Ambulotory Blood Pressure Measurement, irrespective of the indication.

Exclusion criteria

Exclusion criteria: Severe heart rate irregularities of any cause Pregnancy Not able to follow instructions for HBPM or ABPM for any reason

Design outcomes

Primary

Measure	Time frame
Prevalence of the auto-cuff response (defined as a higher average BP on HBPM 10 mmHg systolic or 5 mmHg diastolic compared to daytime ABPM) and their relation to demographic variables, cardiovascular risk factors and target organ damage defined as proteinuria The difference in systolic BP between nocturnal HBPM and ABPM readings (AMSTERDAM at Night substudy).	—

Secondary

Measure	Time frame
- Prevalence of auto-cuff hypertension, defined as having an elevated home BP (135 mmHg systolic or 85 mmHg higher diastolic) and a normal daytime ambulatory BP (defined as	—

Countries

Netherlands

Outcome results