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Different Antiplatelet Therapy Strategy After Coronary Artery Bypass Graft Surgery (DACAB)

4. august 2019 oppdatert av: Qiang Zhao,MD, Ruijin Hospital

Compare the Efficacy of Different Antiplatelet Therapy Strategy After Coronary Artery Bypass Graft Surgery

The study population will include all patients undergoing elective CABG. Consent and randomization will occur before surgery. Total 500 patients undergoing elective CABG will be randomly assigned into three groups with 1:1:1 ratio(167 patients per group) in this open-label study. All the enrolled patients will stop oral antiplatelet drugs according to local protocol before the surgery. Within the first 24 hours after surgery, study medication should be restarted and continued for 12 months. Arm A will restart oral antiplatelet drugs by giving aspirin 100mg qd, Arm B will also restart oral antiplatelet drugs by giving ticagrelor 90mg bid plus aspirin 100mg qd and Arm C will also restart oral antiplatelet drugs by giving ticagrelor 90mg bid. Treatment will continue for 12 months, at which time patients will undergo a multislice computed tomography angiography to assess vein graft patency.

This study is designed to show the superiority of ticagrelor and ticagrelor plus aspirin as compared with aspirin monotherapy respectively for the 1-year primary efficacy end point of vein graft patency.

Studieoversikt

Status

Fullført

Detaljert beskrivelse

The study is designed to show the superiority of ticagrelor and ticagrelor plus aspirin as compared with aspirin monotherapy respectively for the 1-year primary efficacy end point of vein graft patency. The primary comparison includes two separate parts. One is to demonstrate T+A better than A and the other is T better than A.

One year rate of vein graft patency in the aspirin group is estimated as 80%. The assumed rate of ticagrelor plus aspirin is 90%. With a two-sided alpha level 0.05 and 80% power, 199 grafts to each group are required. On the other hand, if we assume the rate of ticagrelor monotherapy has the 1-year vein graft patency rate of 87%, under the same two-sided 0.05 alpha 441 grafts in each arm will offer 80% power to show the superiority of ticagrelor along for the primary efficacy end point.

Combined the above two assumptions, if the allocation rate is 1:1:1, this study needs to recruit 1,323 grafts in total (441 in each) to achieve the pre-specified power for both the two comparisons (T+A vs. A and T vs. A).

The principle investigator assumes that the average number of the vien grafts in one patient is 2.7-3.0. With this assumption, 500 patients are to be recruited, which will provide us a total of 1350 - 1500 grafts.

According to the above, this study will be a confirmatory clinical trial to the primary endpoint.

Studietype

Intervensjonell

Registrering (Faktiske)

500

Fase

  • Fase 4

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Henan
      • Zhengzhou, Henan, Kina
        • Henan Provincial People's Hospital
    • Jiangsu
      • Nanjing, Jiangsu, Kina
        • Jiangsu Province Hospital
      • Nanjing, Jiangsu, Kina
        • Nan Jing First Hospital
    • Shanghai
      • Shanghai, Shanghai, Kina, 200433
        • Changhai Hospital of Shanghai
      • Shanghai, Shanghai, Kina, 200025
        • Ruijin Hospital, Shanghai JiaoTong University School of Medicine
      • Shanghai, Shanghai, Kina, 200092
        • Xinhua Hospital, Shanghai Jiaotong University School of Medicine

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 80 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • Patients able to provide written informed consent
  • Provision of informed consent prior to any study specific procedures
  • Female and male patients aged 18-80 years
  • Indication for CABG surgery

Exclusion Criteria:

  • Cardiogenic shock, haemodynamic instability
  • Need for urgent revascularization within 5 days from presentation
  • Single vessel disease
  • Two vessel disease with normal left ventricular function (> 50%)
  • Need for concomitant other cardiac surgery (e.g. valve replacement)
  • Need for dual antiplatelet treatment for the patients undergoing CABG after acute coronary syndrome(ACS)
  • Contraindication for aspirin and ticagrelor use(e.g. known allergy)
  • History of bleeding diathesis within 3 months prior presentation
  • History of significant GI bleed within 1 year prior presentation
  • History of peptic ulcer without GI bleeding in past 3 years
  • History of intracranial hemorrhage
  • History of moderate to severe liver impairment
  • Patient requires dialysis
  • Patient with an increased risk of bradycardic events (as patients without a pacemaker who have sick sinus syndrome, 2nd or 3rd degree arteriolar-venular block or bradycardic-related syncope)
  • Need vitamin K antagonist therapy after bypass surgery eg. persistent atrial fibrillation, mechanical valves
  • Known, clinically important thrombocytopenia(i.e. < 100*109/L)
  • Known, clinically important anaemia (i.e. <100g/L)
  • Participation in another investigational drug or device study in the last 30 days
  • Pregnancy or lactation(for premenopausal women 2 methods of reliable contraception, one of which must barrier method, are required)
  • Concomitant oral or intravenous therapy with strong cytochrome P450 3A4(CYP3A4) inhibitors, CYP3A4 substrates with narrow therapeutic indices, or strong CYP3A4 inducers which cannot be stopped for the course of the study (strong inhibitors: ketoconazole, itraconazole, voriconazole, telithromycin, clarithromycin, nefazadone, ritonavir, saquinavir, nelfinavir, indinavir, atazanavir, over 1 litre daily of grapefruit juice. Substrates with narrow therapeutic index: cyclosporine, quinidine. Strong inducers: rifampin, phenytoin, carbamazepine. )
  • Any other condition such as active cancer
  • Life expectancy less than 12 months that may result in protocol non-compliance or a risk for being lost to follow up
  • Indication for major surgery(e.g. cancer treatment, carotid surgery, cerebral surgery, major vascular surgery)

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: Aspirin
aspirin 100mg tablet by mouth daily for 12 months
Eksperimentell: Ticagrelor plus Aspirin
ticagrelor 90mg tablet by mouth twice daily and aspirin 100mg tablet by mouth daily for 12 months
Eksperimentell: Ticagrelor
ticagrelor 90mg tablet by mouth twice daily for 12 months

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
The Patency of Saphenous Vein Grafts
Tidsramme: up to 12 months
assessed by multislice computed tomography angiography (MSCTA) or coronary angiography(CAG). FitzGibbon grade A (stenosis <50%) is defined as "patency".
up to 12 months

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
The Patency of Saphenous Vein Grafts
Tidsramme: up to 7 days
assessed by MSCTA or CAG. FitzGibbon grade A (stenosis <50%) is defined as "patency".
up to 7 days
The Rate of Post-operative Atrial Fibrillation After CABG.
Tidsramme: up to 7 days
Number of Participants with Post-operative Atrial Fibrillation after CABG
up to 7 days
The Rate of Freedom From Angina According to Canadian Cardiovascular Society (CCS) Classification
Tidsramme: up to 12 months
Number of Participants Free of Angina per CCS Classification
up to 12 months
The Number of Major Adverse Cardiovascular Event (MACE)
Tidsramme: up to 12 months
MACE, composite of CV death, myocardial infarction or stroke (ischaemic or unknown etiology)
up to 12 months
Number of the Major Bleeding Events
Tidsramme: up to 12 months
According to modified TIMI criteria, the "Major Bleeding Events" is defined as the combination of CABG-related bleeding and non-CABG-related major bleeding(Intracranial bleeding, Clinically overt signs of hemorrhage with hemoglobin drop ≥5 g/dL and Fatal bleeding).
up to 12 months

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
The Rate of Gastroduodenal Injury Assessed by Esophagogastroduodenoscopy (EGD)
Tidsramme: at 12 months
Not all but the patients recruited in Ruijin Hospital
at 12 months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Etterforskere

  • Hovedetterforsker: Qiang Zhao, MD.PhD, Ruijin Hospital Shanghai Jiao Tong University School of Medicine, Shanghai, China
  • Studieleder: Yunpeng Zhu, MD., Ruijin Hospital Shanghai Jiao Tong University School of Medicine, Shanghai, China

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. juli 2014

Primær fullføring (Faktiske)

1. januar 2017

Studiet fullført (Faktiske)

1. januar 2017

Datoer for studieregistrering

Først innsendt

24. juli 2014

Først innsendt som oppfylte QC-kriteriene

24. juli 2014

Først lagt ut (Anslag)

28. juli 2014

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

13. august 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

4. august 2019

Sist bekreftet

1. august 2019

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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