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The Danish On-pump, Off-pump Randomization Study (DOORS)

5. november 2013 opdateret af: Kim Houlind

The Impact of Avoiding Cardiopulmonary By-pass During Coronary Artery Bypass Surgery for Ischemic Heart Disease in Elderly Patients: The Danish On-pump, Off-pump Randomization Study (DOORS)

Background: Coronary artery bypass grafting (CABG) can be performed either with or without the use of cardiopulmonary bypass (CPB) to obtain myocardial re-vascularisation. The investigators hypothesize that CABG without the use of CPB may reduce the risk of perioperative death, stroke, myocardial infarction and other serious complications.

The aim of the present study is to compare the incidence of complications and the clinical efficacy of CABG with and without the use of CPB in elderly patients.

Studieoversigt

Status

Afsluttet

Detaljeret beskrivelse

Conventional coronary artery bypass grafting (CCABG) using cardiopulmonary bypass has for decades been applied to obtain myocardial re-vascularisation and, hence, improved quality of life and survival. It does, however, bear a risk of death, stroke, myocardial infarction and other serious complications.

During recent years, an equivalent operation performed on the beating heart without cardiopulmonary bypass (off-pump coronary artery bypass grafting, OPCAB) has gained popularity helped by the advent of mechanical stabilization devices and improved surgical techniques. Observational studies suggest that this technique is associated with a lower incidence of stroke, per operative arrhythmias and even mortality than conventional CCABG. This is especially the case in elderly patients and patients with significant co-morbidity.

Only few randomised, controlled trials have been conducted and most of these included mainly or only low-risk, relatively young patients. These studies have documented the safety and efficacy of OPCAB compared with CCABG, but none of the trials has had the statistical strength to determine whether the rate of serious complications is lower after OPCAB operations. One recent study found graft patency to be significantly lower after OPCAB than after CCABG operations.

The investigators find that there is a need of a larger scale randomised trial to compare the results of CCABG and OPCAB operations, especially in elderly patients. This patient group is poorly represented in earlier randomised trials, whereas observational studies and theoretical considerations imply that they may benefit the most from avoiding cardiopulmonary bypass.

Aims: Primarily, to compare the incidence of death, stroke and myocardial infarction after CCABG and OPCAB procedures in a population of elderly patients. Furthermore, to compare quality of life and graft patency, and cost- effectiveness after CCABG and OPCAB.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

900

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

      • Aarhus, Danmark, 8200
        • Dept. of Cardiothoracic and Vascular Surgery, Skejby Sygehus, Aarhus University Hospital

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

70 år og ældre (Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Age seventy years or above
  • Admitted for first time coronary artery bypass operation

Exclusion Criteria:

  • Given information cannot be understood
  • Aortic crossclamping not safe due to calcification
  • Preoperative cardiac conditions demanding cardiopulmonary bypass
  • Re-do cardiac surgery
  • Patients requiring operation within the same day after conference

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: CCABG
Coronary artery bypass surgery using cardiopulmonary bypass
Eksperimentel: OPCAB
Coronary artery bypass surgery NOT using cardiopulmonary bypass

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
A combined endpoint of death + stroke + myocardial infarction within 30 days from operation
Tidsramme: 30 days
30 days

Sekundære resultatmål

Resultatmål
Tidsramme
A combined endpoint of death + stroke + myocardial infarction during follow-up
Tidsramme: 3 years
3 years
Patency of bypass grafts assessed by coronary angiography 6 months after the operation
Tidsramme: 6 months
6 months
Total mortality and cardiac mortality during follow-up
Tidsramme: 3 years
3 years
Need of new intervention for cardiac angina during follow-up
Tidsramme: 3 years
3 years
Quality of life assessed by MOS SF-36 and EuroQol questionnaires 6 months and 3 years after the operation
Tidsramme: 6 months and 3 years
6 months and 3 years
Total hospital costs and costs of public care provided 6 months and 3 years after the operation and difference in costs per quality adjusted life year
Tidsramme: 6 months and 3 years
6 months and 3 years

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Efterforskere

  • Ledende efterforsker: Kim C Houlind, MD, PhD, Aarhus University Hospital
  • Studiestol: Poul E Mortensen, MD, Odense University Hospital

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. januar 2005

Primær færdiggørelse (Faktiske)

1. november 2008

Studieafslutning (Faktiske)

1. januar 2011

Datoer for studieregistrering

Først indsendt

25. juli 2005

Først indsendt, der opfyldte QC-kriterier

25. juli 2005

Først opslået (Skøn)

26. juli 2005

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

6. november 2013

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

5. november 2013

Sidst verificeret

1. november 2013

Mere information

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 .

Kliniske forsøg med Iskæmisk hjertesygdom

Kliniske forsøg med Off-Pump Coronary Artery Bypass Grafting

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Abonner