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NCT Number: NCT02464488

New Oral Direct Anticoagulants in Patients 80 Years Old and Over : a Population Pharmacokinetics Study

Several new oral direct anticoagulants have been recently marketed. However, only a few, limited, studies have provided data about the pharmacology of new oral direct anticoagulants in older persons. This study try to better define wether the pharmacology of each of these 3 drugs (dabigatran, rivaroxaban and apixaban) is actually significantly different in very older patients (over 80) and to which extend. The investigators also try to characterize the main determinants (age, weight, renal function, co-morbidities, etc) of the variability observed between individuals in their response to he drugs studied. The method employed is a population pharmacokinetic/pharmacodynamic study.

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Key information

Age range

80 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hôpital Charles Foix, Ivry-sur-Seine, Île-de-France Region, France

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About this study

Several new oral direct anticoagulants have been recently marketed. A main indication for taking these drugs is atrial fibrillation and, in everyday practice, most patients with atrial fibrillation are older people. However, only a few, limited, studies have provided data about the pharmacology of new oral direct anticoagulants in older persons. Furthermore, this limited data strongly suggests that, in older patients, mean concentrations, overall exposition and half-live of these drugs are increased, as compared with younger people. This study try to better define wether the pharmacology of each of these 3 drugs (dabigatran, rivaroxaban and apixaban) is actually significantly different in very older patients (over 80) and to which extend. The investigators also try to characterize the main determinants (age, weight, renal function, co-morbidities, etc) of the variability observed between individuals in their response to he drugs studied. The method employed is a population pharmacokinetic/pharmacodynamic study. This is, many people (projected 225 patients) will have a few blood samples each and all data will be pooled using statistical methods specific to this kind of studies. Each patient will have one to five blood samples, taken at te same time that routine blood analysis, to determine plasma concentrations of the studied drug. In addition, patients will be followed for thrombotic and haemorrhagic events at 6 and 12 months.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 80 years or older
  • Under treatment with dabigatran, rivaroxaban or apixaban
  • For non-valvular atrial fibrillation

Exclusion criteria

  • Mechanical (non-biological) heart valve
  • Any severe condition leading to a short estimated life expectance (a few months)

Treatment and study plan

Plasma drug concentrations

Other

Measure of plasma concentrations of the anticoagulant drug taken by the patient

Primary outcomes

  1. Pharmacologic parameters of new oral anticoagulants in elderly patients

    Time frame: 1 to 3 weeks

    Estimated area under the curve (AUC) of each of the 3 drugs studied

Secondary outcomes

  1. Thromboembolic events

    Time frame: 1 year

    Any thromboembolic event (composite of ischemic stroke, systemic embolism or acute coronary syndrome) in the year after inclusion

  2. Hemorrhagic events

    Time frame: 1 year

    Major hemorrhagic events in the year after inclusion

Sponsors and collaborators

Lead sponsor

Hôpital Charles Foix

Other

Collaborators

  • Assistance Publique - Hôpitaux de Paris
  • Sorbonne University
  • University of Paris 5 - Rene Descartes

Registry information

Official study title

Study of Interindividual Variability in the Response to New Oral Direct Anticoagulants (Dabigatran Etexilate, Rivaroxaban or Apixaban) in Patients 80 Years Old and Over, Using a Population Pharmacokinetics Approach.

Acronym: ADAGE

Important dates

Study start
2015
Primary completion
2021
Study completion
2021
First posted
Jun 8, 2015
Registry last updated
Aug 27, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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