Rivaroxaban Plus Aspirin in Patients With Chronic Coronary Syndrome and High Ischemic Risk

Coronary Artery Disease (CAD) Clinical Trial

Official title:

Effectiveness and Safety of Low Dose Rivaroxaban Plus Aspirin in Patients With Chronic Coronary Syndrome and High Ischemic Risk

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04753372
• Other study ID #: Dutch Rivaroxaban CCS Registry
• Status: Completed
• Start date: December 21, 2020
• Est. completion date: September 13, 2023

Study information

• Verified date: September 2023
• Source: Maatschap Cardiologie Zwolle
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

Registry to describe the impact in terms of effectiveness and safety of the combination treatment of rivaroxaban 2.5 mg twice daily with aspirin on clinical outcomes and practices in a real-life Dutch patient population that are at high risk of ischemic events.

Description:

This study is a national multicentre (~15 sites), prospective, single-arm, observational study in patients treated with rivaroxaban 2.5mg bid on top of ASA75-100mg OD (N=1000). Female and male patients with a diagnosis of CCS and/or symptomatic PAD will be enrolled in the (outpatient) clinic after the decision for treatment with rivaroxaban 2.5mg bid, co-administered with acetylsalicylic acid has been made by the treating physician.

The primary effectiveness endpoint is a composite of:

• Major Adverse Cardiac Events (MACE including stroke, cardiovascular mortality and myocardial infarction)

• Clinically driven coronary, peripheral or carotid revascularization

• Stent thrombosis at one year

The primary safety endpoint is Major Bleeding at one year. These major bleeding complications are analysed according to the International Society on Thrombosis and Haemostasis (ISTH) criteria as a composite of fatal bleeding, symptomatic bleeding into a critical organ (such as intracranial, intraspinal, intraocular, retroperitoneal, intra-articular or pericardial, or intramuscular with compartment syndrome), bleeding causing a fall in haemoglobin level of 2 g/dL (1.24 mmol/L) or more, or leading to transfusion of two or more units of whole blood or red cells.

The secondary endpoints will be:

• Occurrence (and date) of stroke

• Occurrence (and date) of myocardial infarction

• Occurrence (and date) of cardiovascular death

• Occurrence (and date) of coronary revascularization procedures (PCI, CABG).

• Occurrence (and date) of peripheral revascularization procedures.

• Occurrence (and date) of carotid revascularization procedures.

• Occurrence (and date) of minor bleeding complications (according to ISTH)

In addition, all bleeding events including minor bleedings according to ISTH definitions will be reported.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 645
• Est. completion date: September 13, 2023
• Est. primary completion date: September 13, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Adult (=18 years) patient.

• Diagnosis of CAD and/or PAD and high risk of ischemic events.

• Patients at high risk of ischaemic events include the following:

• CAD + PAD

• CAD + Recurrent MI (Previous MI followed by second MI)

• CAD + diabetes mellitus (all types)

• CAD + chronic kidney disease with eGFR 30-59 ml/min/1.73 m2 (CKD-EPI formula)

• CAD + heart failure (ejection fraction =30% - 50%) and New York Heart Association (NYHA) class I or II;)

• CAD + CHA2DS2VaSc = 3 (for men) or = 4 (for women)

• Patients can only be enrolled in the study if the decision to treat with rivaroxaban plus ASA has been made by the treating physician in advance and independent of study inclusion, however within 4 weeks prior to study inclusion.

• Treatment according to local marketing authorization, with rivaroxaban 2.5 mg [BID] and 80mg ASA / 100mg Carbasalate calcium. Treatment of rivaroxaban started within 4 weeks prior or 4 weeks after study inclusion.

• Patients who are willing to participate in this study (signed informed consent).

Exclusion Criteria:

• Hypersensitivity/allergy and known contraindication to ASA/Carbasalate calcium or rivaroxaban

• Patients with recent major bleeding, active bleeding, or history with:

• History of major clinical bleeding or known coagulopathy

• History of intracerebral mass, aneurysm, arteriovenous malformation, or hemorrhagic stroke

• Known severe liver dysfunction

• Patients that have received any organ transplant or await any organ transplant

• Patient with anemia (Hb < 6.0 mmol/L)

• Patient with active malignancy

• Patients with ejection fraction < 30% and/or New York Heart Association (NYHA) class III or IV

• Patients with eGFR < 30 ml/min/1.73m2 or undergoing dialysis

• Patients with liver failure accompanied with coagulopathy ( incl. Child-Pugh B and C)

• Patients with concomitant use of other anticoagulants or antiplatelet drugs

• Pregnant or lactating female

• Patients currently participating in another investigational drug or drug-coated device study

Related Conditions & MeSH terms

• Coronary Artery Disease
• Coronary Artery Disease (CAD)
• Coronary Disease
• Myocardial Ischemia
• Peripheral Arterial Disease
• Peripheral Arterial Disease (PAD)
• Peripheral Vascular Diseases

Intervention

Drug:
• Rivaroxaban 2.5 MG [Xarelto]
rivaroxaban 2.5mg bid on top of ASA for CAD and/or PAD

Locations

Country	Name	City	State
Netherlands	OLVG	Amsterdam
Netherlands	Rijnstate hospital	Arnhem
Netherlands	Jeroen Bosch hospital	Den Bosch
Netherlands	Haaglanden Medisch Centrum	Den Haag
Netherlands	Hagaziekenhuis	Den Haag
Netherlands	Medisch Spectrum Twente	Enschede
Netherlands	Zuyderland Medical Center	Heerlen
Netherlands	Isala Klinieken, location Meppel	Meppel
Netherlands	St. Antonius hospital	Nieuwegein
Netherlands	Elisabeth-Tweesteden hospital	Tilburg
Netherlands	VieCuri	Venlo
Netherlands	Isala hospital	Zwolle

Sponsors (2)

Lead Sponsor	Collaborator
Maatschap Cardiologie Zwolle	Diagram B.V.

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Primary Outcome Measures	The primary efficacy endpoint is a composite of 1) Major Adverse Cardiovascular Events (MACE), which is a composite endpoint of cardiovascular mortality, myocardial infarction and stroke, 2) clinically driven coronary, peripheral or carotid revascularization, and 3) stent thrombosis, that will be reported at 1 year.; The primary safety endpoint is major bleeding according to the International Society on Thrombosis and Haemostatsis (ISTH) criteria that will be reported at 1 year. It is a composite of 1) fatal bleeding, 2) symptomatic bleeding into a critical organ (such as intracranial, intraspinal, intraocular, retroperitoneal, intra-articular or pericardial, or intramuscular with compartment syndrome), 3) bleeding causing a fall in haemoglobin level of 2 g/dL (1.24 mmol/L) or more, or 4) leading to transfusion of two or more units of whole blood or red cells.	one year
Secondary	Secondary Outcome Measures	The secondary efficacy and safety endpoint is the incidence of individual endpoints, that will be reported at 1 year: Occurrence (and date) of stroke; Occurrence (and date) of myocardial infarction; Occurrence (and date) of cardiovascular death; Occurrence (and date) of coronary revascularization procedures (PCI, CABG).; Occurrence (and date) of peripheral revascularization procedures.; Occurrence (and date) of carotid revascularization procedures.; Occurrence (and date) of minor bleeding complications (according to ISTH)	one year