New study checks blood thinner levels in elderly heart patients
NCT ID NCT02894450
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at 70 people aged 75 and older with atrial fibrillation who were taking a Xaban blood thinner (dabigatran, rivaroxaban, or apixaban) during an unplanned hospital stay. Researchers wanted to see if certain clinical or lab factors were linked to higher drug levels in the blood. The goal was to better understand how these medications behave in older patients, not to test a new treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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70 people
The number who actually took part.
- Start date
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Dec 2014
- Finished
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Dec 2015
- Lead sponsor
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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.
Who is studied
All patients over 75 years under anticoagulant treatment 'xaban' (dabigatran, rivaroxaban, Apixaban) for atrial fibrillation, hospital unscheduled manner in Medicine and Geriatric services Versatile Service Home Emergency CHU Nantes and where a hemostatic balance is expected to be offered the study. The recruitment will be made on a 6-month period (November 2014 - April 2015). Bioassay 'xaban' will be made from the remainder of the tube removed for hemostasis tests provided in the usual care of patients.
- Ages
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75 years and older
- Sex
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Anyone
- Healthy volunteers
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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: * Age ≥ 75 years * Entering SAU or MPG (Nantes University Hospital) as part of an unscheduled hospitalization for acute or subacute disease (About MPG, will be included patients admitted to the department within 48 hours of calling the doctor) * In xaban to entry (dabigatran, rivaroxaban, Apixaban) for non-valvular atrial fibrillation * In whom hemostasis tests will be prescribed as part of usual care * Patient has given its verbal agreement Exclusion criteria Patients with the following criteria may not be included: * Patients refusing to participate in the study * Patients under guardianship * Inability to obtain the date and time of the last dose of xaban
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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
-
CHU de Nantes
Nantes, 44093, France
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Other studies related to the condition(s) this trial covers.
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