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NCT05469308Completed

Adherence to Oral Anticoagulants in Patients With Atrial Fibrillation

Predictivity and Evaluation of the Adherence of Ambulatory Patients Treated With a Direct Oral Anticoagulant for Atrial Fibrillation

Source: ClinicalTrials.gov · Last updated 11 Jun 2026

Brief summary (registry, in English)

The rhythm disorders of Atrial Fibrillation (AF) require continuous treatment with anticoagulants to prevent stroke. The introduction of direct oral anticoagulants (DOACs) quickly supplanted the administration of anti-vitamin K (AVK) which presented an elevated risk of hemorrhage. However, the adherence of the treatments by the OAD is very poor, several studies show that 30 to 50% of the patients fail to adhere to their treatment very soon after starting it. In a recent study, in the United States, using data collected between 2010 and 2014 in more than 60,000 patients with AF, Yao et al show that less than 50% of patients can be considered "adherent". They conclude in this study that adherence to anticoagulation is low in practice, although it may be slightly improved with DOACs. More recently a meta-analysis shows that 66% of patient treated by DOACs were considered adherent (PDC \> 80 %). In addition, therapeutic adherence seems to be essential in patients with a CHA2DS2-VASc score ≥2. Indeed improving adherence reduces the risk of stroke occurrence. The investigators propose to evaluate during an interview in the pharmacy, the adherence of ambulatory patients (at the time of their renewal of treatment at the pharmacy) by the "Proportion of Days Covered" (PDC) of the treatment by AOD, and by a simplified questionnaire and to define a profile of patients treated for AF at risk of nonadherence to AOD (PDC adherence prediction score). The investigators perform an observational, prospective multicenter study , in which patients adherence will be quantified in a standardized method.

Status (registry)
Completed
Study type
Interventional
Enrollment
883 (actual)
First submitted
19 Jul 2022
Start date
25 Jan 2022
Primary completion date
18 Jun 2024
Lead sponsor
Centre Hospitalier Universitaire, Amiens
NCT number
NCT05469308

What you commit to

  • Study type: Interventional
  • Participants enrolled: 883
  • From 25 Jan 2022 to the primary completion date, 18 Jun 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Treatment by DOACs limited in the duration
  • Contra-indications of DOACs

Who the study is looking for

  • Over the age of 18
  • Consultation in the community pharmacy
  • long-term treatment for at least six months with an DOACs.
  • Patients able and agreeing to participate in the evaluation of their adherence

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU Amiens
Coordinator of this site? Confirm its status
AmiensFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.