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Clinical Trials/NL-OMON21400
NL-OMON21400
Not yet recruiting
Not Applicable

Functional outcome and quality of life in adult congenital heart disease patients with prosthetic valves (PROSTAVA-study).

etherlands Heart FoundationUniversity Medical Center GroningenICI0 sites600 target enrollmentTBD
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ConditionsProsthetic ValvesAdult Congenital Heart Disease

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Prosthetic Valves
Sponsor
etherlands Heart FoundationUniversity Medical Center GroningenICI
Enrollment
600
Status
Not yet recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

/A

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
etherlands Heart FoundationUniversity Medical Center GroningenICI

Eligibility Criteria

Inclusion Criteria

  • •Adult Congenital Heart Disease patients with a prosthetic heart valve (both homografts,
  • •heterografts and mechanical valves in aortic, mitral, pulmonary or tricuspid position) who are included in the CONCOR database and who give informed consent for the study.

Exclusion Criteria

  • •Inability to comply with primary endpoint measures (completion of quality of life questionary, VO2max). Pregnant patients will not be included, they may be included \> 3 months after pregnancy.

Outcomes

Primary Outcomes

Not specified

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