Clinical Trials Directory

Trials / Recruiting

RecruitingNCT04319627

Statins for Venous Event Reduction in Patients With Venous Thromboembolism

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
2,700 (estimated)
Sponsor
Ottawa Hospital Research Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed description

Recent research has demonstrated that it is plausible that statins have additive, and potentially even synergistic effects, in reducing recurrent VTE in patients managed with anticoagulant-based strategies. Furthermore, it is plausible that statins may reduce the risk of recurrent VTE in those not on anticoagulants and therefore offer an alternative in patients with contraindications to anticoagulants (e.g. after major intracranial bleed), who refuse to take anticoagulants long-term (e.g. due to lifestyle modifications or fear of bleeding) or who cannot afford anticoagulants (e.g. vulnerable or impoverished populations). Finally, statins may also provide protection from recurrent VTE in patients who are not fully compliant with anticoagulant therapy. However, no known RCTs have been done to explore these possibilities. This study aims to determine if generic rosuvastatin reduces the risk of recurrent VTE compared to placebo in patients with symptomatic major VTE. Primary Objectives \- To determine the primary outcome event rate (i.e. symptomatic recurrent major VTE \[proximal DVT or segmental or larger PE\]) in patients taking generic rosuvastatin compared to placebo. Secondary Objectives * To determine the major bleeding event rate in patients taking generic rosuvastatin compared to placebo. * To explore if rosuvastatin reduces the incidence of PTS, as measured by the Villalta scale at end of study.

Conditions

Interventions

TypeNameDescription
DRUGRosuvastatin CalciumEach participant will receive the usual treatment for their newly diagnosed blood clot in addition to the intervention they are randomized to.
DRUGPlacebo Oral TabletEach participant will receive the usual treatment for their newly diagnosed blood clot in addition to the intervention they are randomized to.

Timeline

Start date
2021-02-10
Primary completion
2028-01-01
Completion
2028-04-01
First posted
2020-03-24
Last updated
2026-01-15

Locations

31 sites across 6 countries: Canada, France, Ireland, Italy, Norway, United Kingdom

Source: ClinicalTrials.gov record NCT04319627. Inclusion in this directory is not an endorsement.