Left-Atrium-Appendage Occluder Register - GErmany (LAARGE)
- Evaluation of safety and effectiveness of implantable LAA occluder in clinical practice
- Indication: For which reasons is the indication for implantation of LAA-Occluder put for patients with atrial fibrillation?
- Safety: How save is the implantation of LAA-Occluders?
- Effectiveness: How effective is implantation of LAA-Occluders in daily clinical practice?
- Concomitant treatment: Which concomitant treatment is prescribed for patients with LAA-Occluder?
Studieoversigt
Status
Betingelser
Detaljeret beskrivelse
LAARGE aims to show the care reality of patients whose left atrial appendage (LAA) is closed by an implantable medical device. In particular the following questions should be answered:
- Indication: For which reasons is the indication for implantation of LAA-Occluder put for patients with atrial fibrillation?
- Safety: How save is the implantation of LAA-Occluders (procedural, in hospital and in the long term course)? How frequent are bleeding complications and what is the relation of observed and expected bleeding complications (according HAS-BLED score)?
- Effectiveness: How effective is implantation of LAA-Occluders in daily clinical practice (in hospital and in the long term course)? How frequent are strokes and what is the relation of observed and expected strokes (according CHADS-VASC score)?
- Concomitant treatment: Which concomitant treatment is prescribed for patients with LAA-Occluder?
Undersøgelsestype
Tilmelding (Faktiske)
Kontakter og lokationer
Studiesteder
-
-
-
Coburg, Tyskland, 96450
- Klinikum Coburg
-
Ludwigshafen, Tyskland, 67063
- Institut für Herzinfarkforschung Ludwigshafen
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Mannheim, Tyskland, 68167
- Universitätsmedizin Mannheim
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München, Tyskland, 80331
- Isar Herzzentrum
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
Intention to laa occluder
Exclusion Criteria:
Missing informed consent
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Safety: clinical events with LAA occlusion
Tidsramme: 1 year follow-up (optional 2,3,5 years)
|
Documentation of reasons for LAA Occluder Implantation. Periprocedural and hospital: death, bleeding, pericardial effusion, reanimation, occluder dislocation and further complications. Long term follow-up:: death, bleeding, pericardial effusion, reanimation, occluder dislocation, further complications and patients safety. |
1 year follow-up (optional 2,3,5 years)
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Effectiveness: LAA occlusion
Tidsramme: 1 year follow-up (optional 2,3,5 years)
|
periprocedural and hospital: Sudden or unexpected death, stroke, TIA, systemic embolism, technical success. Long term follow-up: Sudden or unexpected death, stroke, TIA, systemic embolism, patients satisfaction. |
1 year follow-up (optional 2,3,5 years)
|
Samarbejdspartnere og efterforskere
Efterforskere
- Ledende efterforsker: Jochen Senges, MD, Stiftung Institut für Herzinfarktforschung (IHF)
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- LAARGE
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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