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Completed

NCT Number: NCT00224757

Transesophageal Echocardiography to Identify pAtients With Low Risk of Stroke in Atrial Fibrillation - TIARA Pilot Study

In this multi centre pilot study we will perform TEE in patients with AF who are eligible for VKA treatment. TTE will be used as pre-screening: if TTE shows left atrial abnormalities or aortic plaque, patients will be excluded from randomisation. TEE will be performed in all other patients to detect or exclude complex aorta plaques or signs of left atrial stasis. Three hundred patients who do not have these features on TTE will be randomly assigned to treatment with aspirin or VKA. Follow-up will be 1 year.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Jeroen Bosch Ziekenhuis, 's-Hertogenbosch, Netherlands

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About this study

BACKGROUND Atrial fibrillation (AF) is an independent risk factor for stroke. Therapy with vitamin K antagonists (VKA) and aspirin reduces the risk of thromboembolism (TE) dramatically. Risk stratification is nowadays based on clinical characteristics. However, many high risk AF patients may actually be at low risk, identified by trans-oesophageal echocardiography (TEE).

HYPOTHESIS A comprehensive strategy of TEE based aspirin treatment in AF patients eligible for VKA therapy is safe and feasible.

OBJECTIVES

  • To show that TEE based aspirin treatment is safe when compared with VKA therapy.
  • To test the feasibility of TEE as a tool to detect all four echocardiographic features of high stroke risk.

METHODS In this multi centre pilot study we will perform TEE in patients with AF who are eligible for VKA treatment. TTE will be used as pre-screening: if TTE shows left atrial abnormalities or aortic plaque, patients will be excluded from randomisation. TEE will be performed in all other patients to detect or exclude complex aorta plaques or signs of left atrial stasis. Three hundred patients who do not have these features on TTE will be randomly assigned to treatment with aspirin or VKA. Follow-up will be 1 year.

EXPECTED RESULTS Application of a new echo-guided antithrombotic strategy as proposed herein is feasible and may help to reduce bleeding whilst stroke prevention is maintained. If the lower limit of the 95% confidence interval of the yearly incidence of the primary endpoint on aspirin remains below 4.4% then a large multi centre randomised controlled trial will be performed.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Documented atrial fibrillation or atrial flutter, paroxysmal or permanent
  • Conventional indication for VKA treatment
  • Signed informed consent

Exclusion criteria

  • Planned electro cardioversion
  • Very high risk of TE (previous ischemic stroke or systemic TE, symptoms of heart failure or left ventricular dysfunction, mitral valve stenosis, hypertrophic cardiomyopathy)
  • Indication for VKA treatment other than atrial fibrillation (e.g. mechanic valve prosthesis)
  • Atrial fibrillation secondary to reversible diseases (e.g. thyrotoxicosis)
  • Contraindication for treatment with VKA, aspirin, or clopidogrel

Treatment and study plan

Transoesophageal echocardiography

Procedure

TEE

Other names: No other names

Primary outcomes

  1. A composite of the following endpoints: ischemic stroke, systemic embolism, major bleeding, acute coronary syndrome, death.

    Time frame: at least 1 year

Secondary outcomes

  1. Completion of a technical adequate TTE/TEE on the four echocardiographic features of high stroke risk.

    Time frame: 1 year

Sponsors and collaborators

Lead sponsor

The Interuniversity Cardiology Institute of the Netherlands

Other Gov

Registry information

Official study title

Transesophageal Echocardiography to Identify pAtients With Low Risk of Stroke in Atrial Fibrillation

Acronym: TIARA

Important dates

Study start
2005
Primary completion
2009
Study completion
2009
First posted
Sep 23, 2005
Registry last updated
Sep 7, 2011

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

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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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