Comparison Between Direct Oral Anticoagulation (DOAC) Interruption and DOAC Continuation in Patients Undergoing Elective Invasive Coronary Angiography or Percutaneous Coronary Intervention
Recruiting
N/A
Interventional Study
Atrial Fibrillation
Coronary Artery Disease
Anticoagulants
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 1,270 (estimated)
- Sponsor
- Zuyderland Medisch Centrum · Other
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About This Trial
A prospective, multicenter, 1:1 randomized, investigator initiated study. Goal of this study is to examine the safety of uninterrupted periprocedural DOAC use.
Trial Locations
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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 in…
Contacts