Comparison Between Direct Oral Anticoagulation (DOAC) Interruption and DOAC Continuation in Patients Undergoing Elective Invasive Coronary Angiography or Percutaneous Coronary Intervention

NCT ID: NCT04977076

Last Updated: 2021-07-26

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 1214 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-10-01
• Study Completion Date: 2023-12-31

Brief Summary

A prospective, multicenter, 1:1 randomized, investigator initiated study. Goal of this study is to examine the safety of uninterrupted periprocedural NOAC use.

Detailed Description

Rationale: Patients with atrial fibrillation (AF) often have coexisting coronary artery disease (CAD). An estimated 5 to 15% of all AF patients will require coronary stenting. Direct Oral Anticoagulants (DOAC) are more commonly used in preventing thromboembolic complications in patients with AF, thereby substituting the use of Vitamin-K Antagonists (VKA). Therefore, many patients undergoing invasive coronary angiography (ICA) and percutaneous coronary intervention (PCI) are taking direct oral anticoagulants (DOAC). In patients using VKA it is recommended to defer elective coronary angiography until INR is <2.2 when radial artery access is used. However, no large clinical trials have proven the safety of continuing DOAC use when undergoing ICA or PCI. The current guidelines recommend interrupting DOAC treatment at least 24 before ICA or PCI; however, this recommendation is only based on limited data. Clinical decisions on DOAC use must therefore be based on clinical trials in which substantial numbers of patients with Acute Coronary Syndrome (ACS) were included.

Objective: To study the safety of DOAC continuation in patients undergoing ICA or PCI.

Study design: A prospective, multicenter, 1:1 randomized, investigator initiated study.

Study population: Patients aged >18 years using DOAC and undergoing elective ICA or PCI.

Intervention: The intervention group will continue using DOAC as usual. No adjustments of DOAC use will be made before and after ICA or PCI. The control group will receive standard care. DOAC use will be interrupted at least 24-48 hours in advance of ICA or PCI, based on renal clearance and DOAC specimen.

Main study parameters/endpoints: : Non-CABG related in-hospital major bleeding (BARC 3 or 5).

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Only a small burden is associated with participation. Patients are asked to fill out a questionnaire after 30 days. Patients in the control group may have a mildly higher risk of thromboembolic complications and patients in the intervention group may have a mildly higher risk of bleeding complications.

Conditions

Atrial Fibrillation; Coronary Artery Disease; Anticoagulants

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Interrupted NOAC use (group 1)

Patients in group 1 will receive standard care. Therefore, DOAC use will be interrupted at least 24 hours in advance of ICA or PCI. Based on the renal clearance, last DOAC intake may be extended to 48 hours prior to the procedure \[Table 2\]. After the procedure, patients will continue using their DOAC as usual.

Group Type: ACTIVE_COMPARATOR

Interrupted NOAC use

Intervention Type: OTHER

Usual care, interruption of NOAC prior to procedure.

Uninterrupted NOAC use (group 2)

In group 2, all patients will continue to use their specific DOAC as usual. This means that no adjustments of DOAC use will be made before and after ICA or PCI. After the procedure patients will continue to use DOAC from the next planned dose.

Group Type: EXPERIMENTAL

Uninterrupted NOAC use

Intervention Type: OTHER

Continuing NOAC use in advance of elective CAG or PCI.

Interventions

Uninterrupted NOAC use

Continuing NOAC use in advance of elective CAG or PCI.

Intervention Type: OTHER

Interrupted NOAC use

Usual care, interruption of NOAC prior to procedure.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Patients aged >18 years using DOAC and undergoing elective ICA or PCI.
• Provided signed informed consent

Exclusion Criteria

A potential subject who meets any of the following criteria will be excluded from participation in this study:

Any of the following:

• Patients initially presenting with Acute Coronary Syndrome (STEMI, NSTEMI, UA)
• Patients <18 years old
• Calculated CLCR <30 mL/min
• Patients simultaneously participating in another clinical trial
• History or condition associated with increased bleeding risk, as listed below:

• Major surgical procedure within 30 days before the procedure
• Known inaccessible radial artery during previous procedure
• History of GI bleeding in the previous 6 months
• History of intracranial, intraocular, spinal, or atraumatic intra-articular bleeding
• Chronic bleeding disorder
• Known intracranial neoplasm, arteriovenous malformation, or aneurysm
• Known anemia with last measured haemoglobin value <6 mmol/L [9.67 g/dL]
• Current pregnancy or breast-feeding
• Known significant liver disease (e.g., acute clinical hepatitis, chronic active hepatitis, cirrhosis), or ALT >3 x the ULN
• Participation in another clinical trial

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Zuyderland Medisch Centrum

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Central Contacts

Jasper Luijkx, MD

Role: CONTACT

j.luijkx@zuyderland.nl

08854597522

Other Identifiers

METCZ20210099

Identifier Type: -

Identifier Source: org_study_id