← Eichor
Study identifier: NCT04257487 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Sulodexide, VESSEL®, for the Prevention of Recurrent Venous Thromboembolism (The Jason Study)

Condition: Venous Thromboembolism · Anticoagulant · Elderly  ·  Sponsor: Arianna Anticoagulazione Foundation

PhasePhase 3
Planned participants1455
Who can joinAll sexes, 75 Years to no upper limit
Healthy volunteersNo

About this study

The study aims at optimizing extended management of elderly patients (\> 75 years) with at least one of the known bleeding risk factor, who suffered from first episode of venous thromboembolism of the lower extremity (proximal deep vein thrombosis with or without pulmonary embolism) (VTE). Patients were randomized to receive three different treatment: Sulodexide 250 mg BIS in die; Sulodexide 500 BID in die or indistinguishable placebo to verify the efficacy and safety of extended treatment for 12 months with Sulodexide (Vessel®) in the secondary prevention of Deep Vein Thrombosis / Pulmonary Embolism (DVT/PE) recurrence.

This description comes directly from the study's public registry record.

Talk to the study team

Cristina Legnani, BSc, PhD  ·  0039 051 2812339  ·  c.legnani@fondazionearianna.org

Emilia Antonucci, CR  ·  0039 051 4291116  ·  e.antonucci@fondazionearianna.org

Always discuss trial participation with your own doctor first.

Locations (1)

Corrado LodigianiRozzano, ItalyRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT04257487