Long-term mortality after vascular surgery in high-risk patients can be explained through atherothrombotic events en therefore be treated with adequate antithrombotic therapy.
ID
Bron
Verkorte titel
Aandoening
Patients who undergo vascular surgery for abdominal aneurysm or peripheral artery disease who have myocardial injury (e.g. hsTnT release) before and after the procedure.
Patienten die een ingreep ondergaan in verband met een abdominaal aneurysma of perifeer arterieel vaatlijden, met myocard schade (gedefinieerd als hsTnT stijging) voor en na de ingreep.
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The primary objective is to assess the efficacy of clopidogrel, as compared to placebo, on top of standard treatment with aspirin on; <br>
A. the composite endpoint of MACE, defined as;<br>
- cardiovascular death<br>
- non-fatal myocardial infarction<br>
- stroke<br>
- severe ischemia of the coronary or peripheral arterial circulation leading to intervention
Doel van het onderzoek
Long-term mortality after vascular surgery in high-risk patients can be explained through atherothrombotic events en therefore be treated with adequate antithrombotic therapy.
Onderzoeksopzet
T=0: eligibility screening at outpatient clinic visit
T=1: CAG performance to evaluate cardiac risk
T=2a: Vascular Surgery
T=2b: Patient Randomization to study medication
T=3: 30 days after surgery -> first follow-up visit
T=5: 3 months after surgery -> second follow-up visit
T=8: 6 months after surgery -> third follow-up visit
T=11: 9 months after surgery -> fourth follow-up visit
T=14: 12 months after surgery -> fifth follow-up visit
End of study after 1 year of treatment.
Onderzoeksproduct en/of interventie
Clopidogrel or placebo on top of standard treatment with aspirin
Algemeen / deelnemers
Kristin Mol
Postbus 2040
Rotterdam 3000 CA
The Netherlands
Tel.+31 10 704 0 704 / +31 6 26 12 68 30
Email: k.mol@erasmusmc.nl
Wetenschappers
Kristin Mol
Postbus 2040
Rotterdam 3000 CA
The Netherlands
Tel.+31 10 704 0 704 / +31 6 26 12 68 30
Email: k.mol@erasmusmc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Preoperative myocardial injury (baseline value), defined as hsTnT release > 14 ng/L.
2. Absence of significant occlusive coronary artery disease as diagnosed through angiography (and confirmed by FFR).
3. Postoperative myocardial injury, defined as hsTnT release > 14 ng/L, which exceed the baseline value.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Potential subjects will be excluded with any of the following;
1. If event (i.e. hsTnT elevation) is diagnosed as myocardial infarction by cardiologist.
2. Presence of significant occlusive coronary artery disease, as diagnosed through preoperative angiography, requiring treatment.
3. No postoperative hsTnT values above the clinical reference of 14 ng/L and no rise with respect to baseline value.
4. Active bleeding.
5. Active cardiac conditions at the time of randomization such as unstable angina pectoris, active congestive heart failure (CHF), serious cardiac arrhythmias, symptomatic valvular disease.
6. Clear indication for long-term P2Y12 inhibitor use.
7. Preoperative use of P2Y12 inhibitors.
8. Previous allergy or intolerance to clopidogrel.
9. Use of oral anticoagulants after surgery.
10. Use of intravenous glycoprotein IIB/IIIA receptor inhibitors in the previous three days.
11. Coronary revascularization therapy in the previous six months.
12. Renal failure requiring dialysis.
13. Significant liver disease (i.e. ALAT, ASAT > 3x ULN).
14. Cancer with an expected life expectancy less than 6 months.
15. Excessive alcohol use.
16. No informed consent.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL5803 |
| NTR-old | NTR5958 |
| CCMO | NL54577.078.16 |
| OMON | NL-OMON46172 |