Para-Prosthetic Valve Leak Closure Observatory - PVLC2

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age16+
SponsorFondation Hôpital Saint-Joseph

About this trial

Para-prosthetic heart valve leakage is an evolving complication after surgical or percutaneous heart valve replacement. These leaks can lead to heart failure and/or life-threatening hemolysis.

Percutaneous closure of para-prosthetic leaks has developed as an alternative to surgery in high-risk surgical patients. These procedures remain difficult on the technical side with a significant risk of failure and complications but have been improving since the development of dedicated prostheses and the increase in operator experience.

A sharing of experience through the creation of an international expert group has been initiated since 2017 formalised by biannual expert meetings, the elaboration of recommendations in progress and the establishment of an international observatory PVLC1(CCTIRS N°16-62) on 2017-2019.

Beyond the technical aspects and the follow-up of major cardiovascular events collected in PVLC1, the investigators also wonder what impact these procedures have on the quality of life of patients. The investigators suggest that even a partial decrease in para-prosthetic leakage may be associated with an improvement in quality of life by reducing the need for transfusion and/or reducing dyspnea.

A new PVLC2 study is justified to continue the evolutionary follow-up of the technical and clinical results of these procedures, accompanied by the evaluation of the possible benefit on the quality of life of the patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

≥ 16 years and older

Non-opposition of the patient or child's legal representative

Patient referred for a percutaneous para-prosthetic leakage closure procedure

Disqualifiers

≤ 16 years of age

Refusal of the patient to participate in the observatory or the legal representative if the patient is a minor.

Trial population

Patients adressed for a paravalvular leak closure.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • surgical or percutaneous heart valve replacement.

    Procedure/Surgery

    para-prosthetic heart valve leakage after after surgical or percutaneous heart valve replacement

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Evaluate the technical and clinical results of the closure of para-prosthetic leaks by assessing the clinical success of the procedure

Clinical success of the procedure

Time frame
2 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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