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HeartMate II usability in regard to advisories and alarms.

HeartMate II usability in regard to advisories and alarms. - HeartMate II usability

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON31021
Enrollment
28
Registered
2008-03-18
Start date
2008-06-26
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

n.v.t.

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: All ongoing and transplanted Heartmate II patients of the University Medical Center Utrecht who are willing to participate in the study. Thereby a control group of people who are not familiair with the Heartmate II system.

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
The number of errors people make using the HeartMate II system.

Secondary

MeasureTime frame
n/a.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)