Ignite Creation Date:
2025-12-25 @ 12:59 AM
Ignite Modification Date:
2026-01-03 @ 9:01 AM
Study NCT ID:
NCT05506293
Status:
RECRUITING
Last Update Posted:
2022-08-18
First Post:
2022-03-07
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
European Multicentre Registry of Percutaneous Paravalvular Leak Closure
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D006349', 'term': 'Heart Valve Diseases'}], 'ancestors': [{'id': 'D006331', 'term': 'Heart Diseases'}, {'id': 'D002318', 'term': 'Cardiovascular Diseases'}]}}, 'protocolSection': {'designModule': {'studyType': 'OBSERVATIONAL', 'designInfo': {'timePerspective': 'PROSPECTIVE', 'observationalModel': 'COHORT'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 400}, 'targetDuration': '2 Years', 'patientRegistry': True}, 'statusModule': {'overallStatus': 'RECRUITING', 'startDateStruct': {'date': '2020-01-01', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2022-08', 'completionDateStruct': {'date': '2026-07-01', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2022-08-16', 'studyFirstSubmitDate': '2022-03-07', 'studyFirstSubmitQcDate': '2022-08-16', 'lastUpdatePostDateStruct': {'date': '2022-08-18', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2022-08-18', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2024-12-31', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'clinical success', 'timeFrame': '1 year', 'description': 'Device success is a composite criteria including all of the following conditions:\n\nNo rehospitalizations or reinterventions for hemolysis No rehospitalizations or reinterventions for Heart Failure Improvement versus baseline in symptoms defined as decrease in NYHA functional class of at least one class vs. baseline'}], 'secondaryOutcomes': [{'measure': 'clinical success', 'timeFrame': '2 year', 'description': 'Clinical success will be assessed on a composite endpoint at 2 years including the following conditions:\n\n* no death\n* no hospitalization for heart failure,\n* no blood transfusion for hemolysis,\n* no surgical or percutaneous re-intervention on the treated valve.'}, {'measure': 'quality of life', 'timeFrame': '30 days', 'description': 'evolution of quality of life between baseline and 3 months after the procedure on the EQ5D-5L score'}]}, 'oversightModule': {'isUsExport': True, 'oversightHasDmc': True, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['paravalvular leak', 'percutaneous intervention', 'quality of life', 'outcomes'], 'conditions': ['Cardiac Valve Disease', 'Paravalvular Aortic Regurgitation', 'Paravalvular Mitral Regurgitation', 'Paravalvular Leak', 'Quality of Life', 'Outcomes']}, 'descriptionModule': {'briefSummary': 'Paraprosthetic cardiac valve leaks are a progressive complication after after surgical or percutaneous heart valve replacement. These leaks can lead to heart failure and/or life-threatening hemolysis.\n\nPercutaneous closure of para-prosthetic leaks has been developed as an alternative to surgery in high-risk patients. These procedures remain technically challenging with a significant risk of failure and complications, but this risk is improved since the development of dedicated prostheses and the increased experience of the operators. The data in the literature concerning percutaneous leak closure remain limited and disparate and mostly retrospective.The impact of the procedures on the quality of life of patients is not known. Beyond the technical aspects and the follow-up of major cardiovascular events, investigators also wonder what is the impact of these procedures on the quality of life of patients. Investigators hypothesize that even a partial reduction in paraprosthetic leakage may be associated with an improvement in quality of life through reduction of transfusion needs and/or reduction of dyspnea. A prospective study is warranted to assess the technical and clinical and clinical results of these procedures, together with the evaluation of the the possible benefit on the quality of life of the patients.', 'detailedDescription': 'OBJECTIVES OF THE STUDY MAIN OBJECTIVE To evaluate the clinical results of the transcatheter closure of para-prosthetic leaks.\n\nSECONDARY OBJECTIVE Technical success of the procedure defined by successful placement of the prosthesis at the intended site with at least a 1 grade reduction in leakage and residual leakage grade 0-1 Change in quality of life after closure of para-prosthetic leakage at 3 months Evolution of clinical and biological markers of hemolysis and heart failure between at 3 months evolution of clinical markers of functional capacity 4. JUDGMENT CRITERIA 4.1 PRIMARY ENDPOINT\n\n-Clinical success of the procedure:\n\nClinical success will be assessed on a composite endpoint at 2 years:\n\n* vital status,\n* hospitalization for heart failure,\n* blood transfusion for hemolysis,\n* surgical or percutaneous re-intervention on the treated valve. 4.2 SECONDARY ENDPOINTS The technical, echographic, biological and clinical data of the procedure and post procedure will be recorded as well as the complication rates. The EQ5D-5L quality of life score will be evaluated before the procedure, between 1 and 3 months, and post procedure.\n\nSTUDY POPULATION INCLUSION CRITERIA\n\nTo be included, each patient must meet all of the following conditions:\n\n* Patients aged 16 years and older,\n* Patients or the representative of the parental authority of the minor patient who does not object to participation in the observatory,\n* Patients referred for a para-prosthetic leak closure procedure NON-INCLUSION CRITERIA Patients presenting at least one of the following criteria cannot be included\n* Patients under 16 years of age,\n* Refusal of the patient or the representative of the parental authority of the minor patient to participate in the observatory.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD', 'ADULT', 'OLDER_ADULT'], 'maximumAge': '110 Years', 'minimumAge': '16 Years', 'samplingMethod': 'NON_PROBABILITY_SAMPLE', 'studyPopulation': 'Included patients are included as part of their routine clinical care. The percutaneous intervention is not indicated for the purpose of the study but according to each centre policy after a medico-surgical meeting.\n\nPrior to percutaneous intervention, a large investigation of functional status, quality of life, biological exam and echocardiography is performed. This investigation is done again at 1 and 2 years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* ≥16 years of age No opposition from the patient or the representative of the parental authority if the patient is a minor Patient referred for a percutaneous paraprosthetic leak closure procedure\n\nExclusion Criteria:\n\n* \\< 16 years old Refusal of the patient to participate in the observatory or of the legal representative if the patient is a minor'}, 'identificationModule': {'nctId': 'NCT05506293', 'acronym': 'EuroPVL', 'briefTitle': 'European Multicentre Registry of Percutaneous Paravalvular Leak Closure', 'organization': {'class': 'OTHER', 'fullName': 'Centre Chirurgical Marie Lannelongue'}, 'officialTitle': 'European Multicentre Registry of Percutaneous Paravalvular Leak Closure - EuroPVL Study', 'orgStudyIdInfo': {'id': '2019-A02930-57'}}, 'armsInterventionsModule': {'armGroups': [{'label': 'paravalvular leak', 'description': 'patients referred for percutaneous paravalvular leak closure', 'interventionNames': ['Procedure: percutaneous paravalvular leak closure']}], 'interventions': [{'name': 'percutaneous paravalvular leak closure', 'type': 'PROCEDURE', 'otherNames': ['transcatheter paravalvular leak closure'], 'description': 'the procedure consists of deployment of an occluder or a vascular plug within the cardiac paravalvular leak. The device is inserted percutaneously from a femoral vascular approach or from a trans-apical approach. The device is deployed through a delivery sheath within the leak. Stability and efficacy to occlude the leak are assessed by transoesophageal echocardiography prior to device release.\n\nType of devices to be inserted varied :\n\n* Amplatzer vascular plug 3\n* occlutech paravalvular leak device\n* amplatzer vascular plug 2\n* amplatzer muscular ventricular septal defect\n* amplatzer vascular plug 4\n\nDevices to be implanted are under the responsability of the local investigator and are not based on the study design.', 'armGroupLabels': ['paravalvular leak']}]}, 'contactsLocationsModule': {'locations': [{'city': 'Charleroi', 'status': 'RECRUITING', 'country': 'Belgium', 'contacts': [{'name': 'Adel Aminian', 'role': 'CONTACT'}], 'facility': 'CHU Charleroi', 'geoPoint': {'lat': 50.41136, 'lon': 4.44448}}, {'city': 'Třinec', 'status': 'RECRUITING', 'country': 'Czechia', 'contacts': [{'name': 'Jaroslav Januska', 'role': 'CONTACT'}], 'facility': 'Podlesi hospital', 'geoPoint': {'lat': 49.67763, 'lon': 18.67078}}, {'city': 'Amiens', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Laurent Leborgne', 'role': 'CONTACT'}], 'facility': 'CHU Amiens', 'geoPoint': {'lat': 49.9, 'lon': 2.3}}, {'city': 'Annecy', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Lionel Mangin', 'role': 'CONTACT'}], 'facility': 'Hopital d Annecy', 'geoPoint': {'lat': 45.90878, 'lon': 6.12565}}, {'city': 'Créteil', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Emmanuel Teiger', 'role': 'CONTACT'}], 'facility': 'CHU Henri Mondor', 'geoPoint': {'lat': 48.79266, 'lon': 2.46569}}, {'city': 'Grenoble', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Helene Bouvaist', 'role': 'CONTACT'}], 'facility': 'CHU Grenoble', 'geoPoint': {'lat': 45.17869, 'lon': 5.71479}}, {'zip': '92350', 'city': 'Le Plessis-Robinson', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'HASCOET SEBASTIEN, PI', 'role': 'CONTACT', 'email': 's.hascoet@hml.fr', 'phone': '+33140942429'}], 'facility': 'centre chirurgical Marie Lannelongue', 'geoPoint': {'lat': 48.78889, 'lon': 2.27078}}, {'city': 'Lille', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Regis Ketelers', 'role': 'CONTACT'}], 'facility': 'Hopital Prive Brabois', 'geoPoint': {'lat': 50.63391, 'lon': 3.05512}}, {'city': 'Marseille', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Guillaume Bonnet', 'role': 'CONTACT'}], 'facility': 'CHU La Timone', 'geoPoint': {'lat': 43.29695, 'lon': 5.38107}}, {'city': 'Marseille', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Sebastien Armero', 'role': 'CONTACT'}], 'facility': 'Hopital Europeen', 'geoPoint': {'lat': 43.29695, 'lon': 5.38107}}, {'city': 'Marseille', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Frederic Collet', 'role': 'CONTACT'}], 'facility': 'Hopital Prive Clairval', 'geoPoint': {'lat': 43.29695, 'lon': 5.38107}}, {'city': 'Nancy', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Batric Popovic', 'role': 'CONTACT'}], 'facility': 'CHU Nancy', 'geoPoint': {'lat': 48.68439, 'lon': 6.18496}}, {'city': 'Nîmes', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Vlad Ciobotaru', 'role': 'CONTACT'}], 'facility': 'Hopital prive les Franciscaines', 'geoPoint': {'lat': 43.83665, 'lon': 4.35788}}, {'city': 'Paris', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Christian Spaulding', 'role': 'CONTACT'}], 'facility': 'HEGP', 'geoPoint': {'lat': 48.85341, 'lon': 2.3488}}, {'city': 'Paris', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Eric Brochet', 'role': 'CONTACT'}, {'name': 'Gregory Ducrocq', 'role': 'CONTACT'}], 'facility': 'Hopital Bichat', 'geoPoint': {'lat': 48.85341, 'lon': 2.3488}}, {'city': 'Paris', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Nadjib Hammoudi', 'role': 'CONTACT'}], 'facility': 'Hopital Pitie Salpetriere', 'geoPoint': {'lat': 48.85341, 'lon': 2.3488}}, {'city': 'Rennes', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Guillaume Leurent', 'role': 'CONTACT'}], 'facility': 'CHU Rennes', 'geoPoint': {'lat': 48.11109, 'lon': -1.67431}}, {'city': 'Rouen', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Fabrice Bauer', 'role': 'CONTACT'}], 'facility': 'Hopital Charles Nicolle', 'geoPoint': {'lat': 49.44313, 'lon': 1.09932}}, {'city': 'Saint-Denis', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Mohammed Nejjari', 'role': 'CONTACT'}], 'facility': 'Centre Cardiologique du Nord', 'geoPoint': {'lat': 48.93564, 'lon': 2.35387}}, {'city': 'Saint-Laurent-du-Var', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Emmanuelle Arigon', 'role': 'CONTACT'}], 'facility': 'institut Arnault Tzanck', 'geoPoint': {'lat': 43.67323, 'lon': 7.19}}, {'city': 'Toulouse', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Frederic Bouisset', 'role': 'CONTACT'}], 'facility': 'CHU Toulouse', 'geoPoint': {'lat': 43.60426, 'lon': 1.44367}}, {'city': 'Toulouse', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Nicolas Combes', 'role': 'CONTACT'}], 'facility': 'Clinique Pasteur', 'geoPoint': {'lat': 43.60426, 'lon': 1.44367}}, {'city': 'Villeurbanne', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Didier Champagnac', 'role': 'CONTACT'}], 'facility': 'Medipole Lyon Villeurbanne', 'geoPoint': {'lat': 45.76601, 'lon': 4.8795}}, {'city': 'Athens', 'status': 'RECRUITING', 'country': 'Greece', 'contacts': [{'name': 'Carmen Moldovan', 'role': 'CONTACT'}], 'facility': 'National and kapodistrian university of athens', 'geoPoint': {'lat': 37.98376, 'lon': 23.72784}}, {'city': 'Milan', 'status': 'RECRUITING', 'country': 'Italy', 'contacts': [{'name': 'Eustaquio Onorato', 'role': 'CONTACT'}], 'facility': 'University School of Milan', 'geoPoint': {'lat': 45.46427, 'lon': 9.18951}}, {'city': 'Riga', 'status': 'RECRUITING', 'country': 'Latvia', 'contacts': [{'name': 'Ainars Rudzitis', 'role': 'CONTACT'}], 'facility': 'Pauls Stradins Clinical University Hospital', 'geoPoint': {'lat': 56.946, 'lon': 24.10589}}, {'city': 'Vilnius', 'status': 'RECRUITING', 'country': 'Lithuania', 'contacts': [{'name': 'Aleksejus Zorinas', 'role': 'CONTACT'}], 'facility': 'Vilnius University Hospital', 'geoPoint': {'lat': 54.68916, 'lon': 25.2798}}, {'city': 'Mexico City', 'status': 'RECRUITING', 'country': 'Mexico', 'contacts': [{'name': 'Juan Pablo Sandoval', 'role': 'CONTACT'}], 'facility': 'hospital infantil de Mexico Frederico Gomez', 'geoPoint': {'lat': 19.42847, 'lon': -99.12766}}, {'city': 'Katowice', 'status': 'RECRUITING', 'country': 'Poland', 'contacts': [{'name': 'Grzegorz Smolka', 'role': 'CONTACT'}], 'facility': 'Medical University of Silesia', 'geoPoint': {'lat': 50.2597, 'lon': 19.02173}}, {'city': 'Barcelona', 'status': 'RECRUITING', 'country': 'Spain', 'contacts': [{'name': 'Xavier Freixa', 'role': 'CONTACT'}], 'facility': 'Hospital Clinic of Barcelona', 'geoPoint': {'lat': 41.38879, 'lon': 2.15899}}, {'city': 'Kocaeli', 'status': 'RECRUITING', 'country': 'Turkey (Türkiye)', 'contacts': [{'name': 'Teoman Kilic', 'role': 'CONTACT'}], 'facility': 'Kocaeli University Medical Faculty', 'geoPoint': {'lat': 39.62497, 'lon': 27.51145}}, {'city': 'Cambridge', 'status': 'RECRUITING', 'country': 'United Kingdom', 'contacts': [{'name': 'Patrick Calvert', 'role': 'CONTACT'}], 'facility': 'Royal Papworth hospital', 'geoPoint': {'lat': 52.2, 'lon': 0.11667}}, {'city': 'Edinburgh', 'status': 'RECRUITING', 'country': 'United Kingdom', 'contacts': [{'name': 'Behan Miles', 'role': 'CONTACT'}], 'facility': 'Edinburgh Royal Infirmary', 'geoPoint': {'lat': 55.95206, 'lon': -3.19648}}], 'centralContacts': [{'name': 'Sebastien Hascoet, MD, PhD', 'role': 'CONTACT', 'email': 's.hascoet@ghpsj.fr', 'phone': '0033140942429'}, {'name': 'Benoit Gerardin, MD', 'role': 'CONTACT', 'email': 'b.gerardin@ghpsj.fr'}], 'overallOfficials': [{'name': 'Sebastien Hascoet, MD, PhD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 's.hascoet@ghpsj.fr'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Centre Chirurgical Marie Lannelongue', 'class': 'OTHER'}, 'collaborators': [{'name': 'Easy-CRF', 'class': 'UNKNOWN'}], 'responsibleParty': {'type': 'SPONSOR'}}}}