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Functional outcome and quality of life in adult congenital heart disease patients with prosthetic valves*

Functional outcome and quality of life in adult congenital heart disease patients with prosthetic valves* - Prostava

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON32722
Enrollment
600
Registered
2010-05-21
Start date
2010-11-13
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

prosthetic heart valves in congenital heart disease

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Included in concor database, congenital heart disease, valve prosthesis 9all required)

Exclusion criteria

Exclusion criteria: Inability to comply with examinations (quality of life questionnaire and exercise test)

Design outcomes

Primary

MeasureTime frame
Primary outcomes are VO2max and quality of life.

Secondary

MeasureTime frame
Secondary outcomes are the prevalence of PPM and the incidence of valve related complications.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)