- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00176397
Percutaneous Coronary Intervention (PCI) With Drug-Eluting Stents (DES) Versus Coronary Artery Bypass Graft (CABG) for Patients With Significant Left Main Stenosis
PCI With DES Versus CABG for Patients With Significant Left Main Stenosis
Recent technical advances in percutaneous coronary interventions have made it possible to approach patients with coronary lesions formerly considered to be classical candidates for bypass surgery, e.g. patients with left main coronary stenosis. However, it is still unclear whether the good long-term results achieved with the surgical therapy can be reproduced by an interventional strategy using drug-eluting stents (DES).
The aim of the current trial is, therefore, to compare the clinical and angiographic results of PCI and CABG in patients with left main coronary stenosis.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Recent technical advances in percutaneous coronary interventions have made it possible to approach patients with coronary lesions formerly considered to be classical candidates for bypass surgery, e.g. patients with left main coronary stenosis. However, it is still unclear whether the good long-term results achieved with the surgical therapy can be reproduced by an interventional strategy using drug-eluting stents (DES).
The aim of the current trial is, therefore, to compare the clinical and angiographic results of PCI and CABG in patients with left main coronary stenosis.
The study was planned as a "non-inferiority" trial based on the hypothesis that PCI may be able to reach similar long-term results as compared to CABG.
Undersøgelsestype
Tilmelding (Forventet)
Fase
- Fase 2
Kontakter og lokationer
Studiesteder
-
-
Saxony
-
Leipzig, Saxony, Tyskland, 04289
- Rekruttering
- University of Leipzig, Heart Center
-
Kontakt:
- Enno Boudriot, MD
- Telefonnummer: 1428 +49-341-865
- E-mail: boue@medizin.uni-leipzig.de
-
Kontakt:
- Gerhard Schuler, MD
- Telefonnummer: 1428 +49-341-865
- E-mail: schug@medizin.uni-leipzig.de
-
Underforsker:
- Enno Boudriot, MD
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Significant left main coronary stenosis >= 50%
Exclusion Criteria:
- Acute myocardial infarction (STEMI < 48h)
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
|---|
|
Major adverse coronary events (cardiac death, myocardial infarction, need for repeat revascularisation)
|
Sekundære resultatmål
Resultatmål |
|---|
|
Functional status (CCS-class)
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Studieleder: Gerhard Schuler, MD, University of Leipzig
- Studieleder: Friedrich Mohr, MD, University of Leipzig
Datoer for undersøgelser
Studer store datoer
Studiestart
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 118/2003
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .