Can dropping one blood thinner cut bleeding without raising heart risks?
NCT ID NCT04250116
First seen Sep 01, 2026 · Last updated Sep 04, 2026 · Updated 2 times
Summary
This trial tests whether people with atrial fibrillation who had a stent placed more than a year ago can safely switch from two blood thinners to just one. Participants receive either a single anticoagulant or the same anticoagulant plus clopidogrel for two years. Researchers track deaths, heart attacks, strokes, and bleeding to see which strategy offers the better balance of protection and safety.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A single anticoagulant (apixaban, rivaroxaban, or warfarin) compared with the same anticoagulant plus clopidogrel
- What this could lead to
- If a single blood thinner works as well as dual therapy, patients could avoid extra bleeding risk while keeping stroke and stent protection.
- What could go wrong
- This is a Phase 4 trial, so the approach is already used in practice, but the optimal long-term strategy is unproven. Single therapy might raise the risk of stent clots or heart attacks.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
960 people
The number who actually took part.
- Started
-
Apr 2020
- Finished
-
May 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
19 to 85 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. over 19 years old 2. Patient who underwent PCI with DES more than 12 months ago 3. Non-valvular atrial fibrillation patients requiring long-term anticoagulation Exclusion Criteria: 1. Over 85 years old 2. Pregnancy or Potential Pregnancy 3. Life expectancy within 1 year 4. Patients who refuse or do not understand the written consent form 5. Requiring anticoagulation due to history of mechanical valve replacement, mitral stenosis or deep vein thrombosis 6. Coagulopathy, continuous bleeding, or Hb level below 10 g/dL 7. Intracerebral hemorrhage within 2 months 8. Patients with gastrointestinal hemorrhage within three months of registration 9. Patients diagnosed with a gastrointestinal tumor that requires continuous treatment 10. Patients treated with 1st generation drug-eluting stents (Cypher, Taxus, or Endeavor Sprint)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Severance Cardiovascular Hospital, Yonsei University Health System
Seoul, South Korea
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Other studies related to the condition(s) this trial covers.
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