Post Thrombotic Syndrome

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Review clinical trials related to Post Thrombotic Syndrome. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

DEFIANCE: RCT of ClotTriever System Versus Anticoagulation In Deep Vein Thrombosis

This study is a prospective, multicenter, randomized controlled trial of an interventional strategy using the ClotTriever System to achieve and maintain vessel patency (ClotTriever Intervention Arm) versus conservative medical management using anticoagulation therapy alone (Conservative Medical Management Arm) in the treatment of subjects with symptomatic unilateral iliofemoral DVT. The study will collect data on demographics, comorbidities, details from the DVT diagnosis and treatment, and clinical outcomes through the 6-month follow up visit.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Inari MedicalUpdated: Jul 2, 2026Locations: 64
Eligibility criteria

Age ≥ 18 years [+4]

Bilateral iliofemoral DVT [+20]

Status: Not yet recruiting

Incidence and Characteristic of CRT Persistent After Catheter Extraction in ICU Patients

The goal of this observational study is to describe characteristics of catheter related thrombosis (CRT) that persists after catheter extraction in condition of intensive care unit. The main questions it aims to answer are: 1. What is the incidence of CRT that persists after catheter extraction in patients hospitalized in the intensive care unit? 2. What are the risk factors for this phenomenon? 3. What is the fate of such a thrombus, including recanalization or the development of complications such as pulmonary embolism or post-thrombotic syndrome?

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Masarykova Nemocnice v Usti nad Labem, Krajska Zdravotni a.s.Updated: Mar 16, 2026
Eligibility criteria

age over 18 years [+3]

age under 18 years [+2]

Status: Not yet recruiting

Design and Rationale of the COLT Study

Deep vein thrombosis (DVT) is a condition in which a blood clot forms in the deep veins of the leg and can lead to long-term problems such as leg pain, swelling, and reduced quality of life. Standard treatment with blood-thinning medication lowers the risk of complications, but some patients still develop long-term damage to the veins. Inflammation is thought to play an important role in these complications. This study will evaluate whether adding colchicine, an anti-inflammatory medication already used for other conditions, to standard anticoagulant therapy can improve outcomes in patients with acute DVT. Participants will be randomly assigned to receive either colchicine or a placebo, in addition to usual blood-thinning treatment, and will be followed for one year. The main goal of the study is to determine whether colchicine reduces the risk of developing long-term vein problems after DVT. The study will also assess the risk of new blood clots, vein recovery, quality of life, and the safety of colchicine treatment.

Participants needed: 940
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Azienda Sanitaria Locale ASL 6, LivornoUpdated: Feb 25, 2026
Eligibility criteria

Age ≥18 years at the time of screening. [+5]

History of prior DVT in the same limb. [+14]

Status: Recruiting

Statins for Venous Event Reduction in Patients With Venous Thromboembolism

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.

Participants needed: 2,700
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Ottawa Hospital Research InstituteUpdated: Jan 15, 2026Locations: 31
Eligibility criteria

Unable or unwilling to provide written informed consent; [+24]

Status: Not yet recruiting

Immunosuppressive Therapy Alone Versus Plus Oral Anticoagulation in the Treatment of VT Associated With Behcet's Disease

This study is a Phase III, multicenter, prospective, randomized, double-blind, placebo-controlled clinical trial investigating the treatment of lower extremity venous thrombosis associated with Behçet's Disease. The study compares the effectiveness and safety of immunosuppressive therapy alone versus immunosuppressive therapy combined with oral anticoagulation (Rivaroxaban).

Participants needed: 110
Trial details
Phase: Phase 3Age: 18-50Biological sex: AllType: InterventionalSponsor: Marmara UniversityUpdated: Apr 13, 2025Locations: 2
Eligibility criteria

Not listed