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Clinical Trials in Ireland / NCT04319627
Recruiting Phase 3

Statins for Venous Event Reduction in Patients With Venous Thromboembolism

NCT04319627 · tracked via the Priya Life Science Ireland tracker
Sponsor
Ottawa Hospital Research Institute
Phase
Phase 3
Started
2021-02-10
Last updated
2026-01-15

Condition(s) studied

Venous ThromboembolismBlood ClotPost Thrombotic Syndrome

Investigational drug(s) / intervention(s)

Rosuvastatin CalciumPlacebo Oral Tablet

Rosuvastatin Calcium: Each participant will receive the usual treatment for their newly diagnosed blood clot in addition to the intervention they are randomized to.

Placebo Oral Tablet: Each participant will receive the usual treatment for their newly diagnosed blood clot in addition to the intervention they are randomized to.

Study summary

The standard or usual treatment for patients diagnosed with deep vein thrombosis or pulmonary embolism is treatment with blood thinners (called anticoagulants).

While treatment of blood clots with blood thinners is effective, some research has shown that adding a statin (medication used to lower cholesterol) may give extra protection. It is thought that statins can improve how cells along the walls of the vein control inflammation, which can prevent new blood clots from forming.

The medication in this study, rosuvastatin, is approved in Canada for use as a cholesterol-lowering medication. The use of rosuvastatin in this study is considered investigational. This means that Health Canada has not approved the use of rosuvastatin as a treatment for blood clots. However, it has been approved for use in this research study.

The purpose of this study is to examine if adding a statin (rosuvastatin) to the usual blood thinner treatment will decrease the risk of another blood clot forming. The investigators also hope to discover if taking a statin reduces damage to your veins. To do this, some of the participants in this study will get rosuvastatin and others will receive a placebo (a substance that looks like the study rosuvastatin but does not have any active or medicinal ingredients). The placebo in this study is not intended to have any effect on your blood clot. A placebo is used to make the results of the study more reliable.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: 1\. Symptomatic objectively confirmed proximal leg DVT (above the trifurcation of the popliteal vein) and/or PE (segmental or greater) diagnosed in the last 30 days. Exclusion criteria 1. Unable or unwilling to provide written informed consent; 2. \< 18 years of age; 3. Women of childbearing potential unwilling to use appropriate contraception; 4. Currently prescribed a statin; 5. A known medical history or current diagnosis of any of the following for which statins are indicated in secondary prevention: 1. Diabetes; 2. Abdominal aortic aneurysm; 3. Peripheral arterial disease; 4. Stroke; 5. Transient ischemic attack (TIA); 6. Myocardial infarction (MI); 7. Acute coronary syndromes; 8. Stable/unstable angina; 9. Coronary or other arterial revascularization; 6. Known diagnosis of hypercholesterolemia or dyslipidemia; 7. Contraindication to rosuvastatin; 1. Known hypersensitivity or intolerance to statins; 2. History of muscle disorders or statin-related muscle pain; 3. Known liver disease (active liver disease, e.g. Hepatitis A, B, C, non-alcoholic fatty liver); 4. Chronic kidney disease (creatinine clearance \< 30ml/min); 5. Currently pregnant or breast feeding; 6. Taking cyclosporine; 7. Taking atazanavir/ritonavir; 8. Taking darolutamide; 9. Taking regorafenib; 8. Unstable medical or psychological condition that would interfere with trial participation.

Primary outcome measure(s)

Trial sites (31)

FacilityCityRegionStatus
Foothills Medical Centre Calgary Alberta Recruiting
Queen Elizabeth II Hospital Halifax Nova Scotia Withdrawn
Hamilton General Hospital Hamilton Ontario Recruiting
St. Joseph's Healthcare Hamilton Ontario Recruiting
Juravinski Hospital Hamilton Ontario Withdrawn
The Ottawa Hospital Ottawa Ontario Recruiting
Hôpital Montfort Ottawa Ontario Withdrawn
Niagara Health - St. Catharines Site St. Catharines Ontario Recruiting
Sunnybrook Hospital Toronto Ontario Not Yet Recruiting
University Health Network Toronto Ontario Recruiting
Jewish General Hospital Montreal Quebec Recruiting
McGill Univeristy Health Centre Montreal Quebec Recruiting
CIUSSS de-l'Ouest-de-l'Ile-de-Montreal -St. Mary's Hospital Center Montreal Quebec Recruiting
CHU de Quebec-Université Laval Québec Quebec Recruiting
CHU d'Angers - Service d'accueil et traitement des Urgences Angers France Recruiting
Brest University Hospital Centre Brest France Recruiting
CHU de Clermont-Ferrand, Hôpital Gabriel Montpied Clermont-Ferrand France Recruiting
APHP Hôpital Louis Mourier Colombes France Recruiting
CHU de Dijon - Service d'imagerie diagnostique et thérapeutique Dijon France Recruiting
GH La Rochelle - Ré-Aunis - Service de Médecine vasculaire La Rochelle France Recruiting
Centre Hospitalier Universitaire De Saint Etienne Saint-Etienne France Recruiting
CHI Toulon - La Seyne sur Mer - Hôpital Sainte Musse Toulon France Recruiting
Mater Misericordiae University Hospital Dublin Ireland Not Yet Recruiting
University of Insubria Varese Italy Not Yet Recruiting
Ostfold Hopsital Sarpsborg Norway Recruiting
Aberdeen Royal Infirmary Aberdeen United Kingdom Not Yet Recruiting
Queen Elizabeth Hospital Birmingham United Kingdom Not Yet Recruiting
University Hospital of Wales Cardiff United Kingdom Not Yet Recruiting
Glasgow Royal Infirmary Glasgow United Kingdom Not Yet Recruiting
King's College Hospital NHS Foundation Trust London United Kingdom Not Yet Recruiting
Oxford University Hospitals NHS Foundation Trust Oxford United Kingdom Not Yet Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04319627 on ClinicalTrials.gov ↗ ← All trials in Ireland