- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01310725
Evaluation of Graft Material in Coronary Artery Bypass Grafting (CABG)
Mid-term Patency of Radial Artery and No Touch Saphenous Vein as Grafts in CABG; A Randomised Controlled Trial.
The aim of the study is to evaluate the patency in different kinds of vessels used as graft material in coronary artery bypass grafting.
The hypothesis is that vein grafts harvested with a pedicle of surrounding tissue have the same, or better, patency compared to radial grafts and that skeletonisation of the left internal mammary artery does not effect the patency for this graft.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Patients undergoing coronary artery bypass grafting are included in the study.
Each patient receive a radial artery graft and a vein graft harvested with a pedicle of surrounding tissue to the right and left side of the heart respectively. The left internal mammary artery is used for the left anterior descending artery in a skeletonised or non-skeletonised fashion.
The evaluation is made with angiography up to 5 years after surgery.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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-
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Orebro, Sverige, 701 85
- Dept of Cardiothoracic Surgery, Orebro University Hospital
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Isolated coronary artery disease embracing all three main branches of the coronary artery tree.
Exclusion Criteria:
- Kidney insufficiency (Creatinine > 120 µmol/L)
- War-farin anticoagulation therapy
- Ejection fraction < 40%
- Repeat operation
- Other concurrent sur-gery
- Signs of reduced circulation in non-dominant hand
- Other severe illness, or if the patient declines to participate.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Enkelt gruppeopgave
- Maskning: Enkelt
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
Functional grafts defined as opened or closed.
Tidsramme: Up to 5 years after surgery.
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Up to 5 years after surgery.
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
---|---|
Degree of stenosis in implanted grafts.
Tidsramme: Up to 5 years after surgery.
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Up to 5 years after surgery.
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Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Studiestol: Lars Norgren, MD, PhD, Prof., Örebro University
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 (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- mdr001
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