LVT DURATION: Pilot Study of Anticoagulation Duration for Left Ventricular Thrombus

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorQueen Mary University of London

About this trial

The LVT DURATION (Optimal Duration of Anticoagulation for LV Thrombus) is a pilot study planned to assess the practicalities of conducting a randomised control trial (RCT) whilst establishing data around the ideal duration of anticoagulation in the treatment of LV thrombus. The main objectives of the study are:

* To assess the practicalities of conducting an RCT with regard to recruitment, retention, and outcome measurement. * To identify the optimal length of anticoagulation in the treatment of LV Thrombus

After randomisation participants will:

* Continue their prescribed oral anticoagulant for the remainder of the trial * Discontinue their prescribed oral anticoagulant for the remainder of the trial

Eligibility criteria

Qualifiers

Diagnosis of LV thrombus less than 12 months ago

On Apixaban at the time of randomisation

Completed at least 3 months of anticoagulation treatment for LV thrombus

Persistent laminar/ mural thrombus or persistent LV dysfunction

Disqualifiers

Any clinical condition requiring long term anticoagulation treatment as per investigator's judgement.

SSE since LV thrombus diagnosis

Contraindication to continuing anticoagulation therapy

Non-ischaemic Cardiomyopathy

Trial design

Treatments tested in this trial

  • Continue rivaroxaban or apixaban or warfarin
  • Discontinue rivaroxaban or apixaban or warfarin

Treatment groups

120 Participants
are divided into 2 treatment groups