Non-invasive continuous blood pressure monitoring in critically ill patients

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00004411

Enrollment

Registered

2012-09-27

Start date

2009-12-04

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

Critically ill patients with indwelling arterial catheters who need continuous blood pressure monitoring

Interventions

Group 1: 25 patients. Both methods (NEXFIN vs. invasive intra-arterial blood pressure monitoring) will be compared in the same subject

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Critically ill patients with indwelling arterial catheters for invasive arterial blood pressure monitoring.

Exclusion criteria

Exclusion criteria: marked haemodynamic instability cardiac arrhythmia ischemia of the fingers

Design outcomes

Primary

Measure	Time frame
Comparison of mean arterial pressure obtained by two different methods at 5 different time points at 0 and after 1, 2, 3, 4h. NEXFIN vs. invasive intra-arterial blood-pressure	—

Secondary

Measure	Time frame
Comparison of systolic arterial pressure obtained by two different methods at 5 different time points at 0 and after 1, 2, 3, 4h. NEXFIN vs. invasive intra-arterial blood-pressure	—

Countries

Germany

Contacts

Public ContactAndreas Hohn

Krankenhaus Düren

hohna@web.de02421-301396

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026