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Thrombosis clinical trials

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NCT ID: NCT05081375 Terminated - Surgical Blood Loss Clinical Trials

Pre-operative Enoxaparin in the Surgical Management of Multi-trauma Patients Undergoing Orthopedic Surgical Procedures

Start date: December 16, 2019
Phase: Phase 4
Study type: Interventional

All trauma patients receive Lovenox or other prophylactic medication to prevent deep vein clots from forming. For the trauma patients with orthopedic injuries requiring surgery there is controversy over safety and efficacy when prophylaxis is started preoperatively vs postoperatively. This study is to evaluate both approaches for safety in terms of bleeding events during and 24 hours after surgery as well as preventing deep vein clot formation. This will be a randomized double blinded study using Lovenox or placebo as the medications given preoperatively. Postoperative Lovenox will be given to both groups per routine regime.

NCT ID: NCT04920929 Terminated - Peripheral ICC Clinical Trials

PICC Asymptomatic Thrombosis Study: A Pilot Study

Start date: July 15, 2021
Phase: N/A
Study type: Interventional

The study purpose is to perform a preliminary, comparative evaluation of the Hydrophilic Biomaterial technology to confirm the performance of the catheter, by using UltraSound technology in-vivo.

NCT ID: NCT04794569 Terminated - Clinical trials for Deep Vein Thrombosis

Tinzaparin Lead-In to Prevent the Post-Thrombotic Syndrome

TILE
Start date: November 15, 2021
Phase: Phase 4
Study type: Interventional

The TILE pilot study will be a multicenter, open-label, assessor-blinded RCT (randomized control trial) comparing extended LMWH (Low Molecular Weight Heparin) vs. DOAC (Direct Oral Anticoagulants) to PTS (prevent post thrombotic syndrome) in patients with DVT (Deep Vein Thrombosis).

NCT ID: NCT04746339 Terminated - Covid19 Clinical Trials

Apixaban for PrOphyLaxis of thromboemboLic Outcomes in COVID-19

APOLLO
Start date: March 4, 2021
Phase: Phase 4
Study type: Interventional

Randomized, double-blinded, placebo-controlled trial comparing oral anticoagulation with placebo for community-dwelling patients with symptomatic COVID-19 infection and risk factors for thrombosis.

NCT ID: NCT04498273 Terminated - COVID-19 Clinical Trials

COVID-19 Positive Outpatient Thrombosis Prevention in Adults Aged 40-80

Start date: September 7, 2020
Phase: Phase 3
Study type: Interventional

A multi-center adaptive randomized placebo-controlled platform trial evaluating the efficacy and safety of anti-thrombotic strategies in COVID-19 adults not requiring hospitalization at time of diagnosis

NCT ID: NCT04494035 Terminated - Clinical trials for Arteriovenous Graft Thrombosis

AVATR - Arteriovenous Access Thrombosis Removal With CAPERE Thrombectomy System

AVATR
Start date: January 14, 2020
Phase: N/A
Study type: Interventional

A prospective, single-arm, non-blinded study, intending to treat and collect and evaluate data in up to ten (10) human subjects who are currently being treated with hemodialysis and who present with acute thrombosis in their arteriovenous (AV) grafts, treated with the CAPERE® Thrombectomy System.

NCT ID: NCT04465760 Terminated - Lymphoma Clinical Trials

Xisomab 3G3 for the Prevention of Catheter-Associated Thrombosis in Patients With Cancer Receiving Chemotherapy

Start date: February 25, 2021
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well xisomab 3G3 works in preventing catheter-associated blood clots (thrombosis) in patients with cancer receiving chemotherapy. Many patients with cancer develop blood clots from their catheters and can have pain, swelling, and other symptoms. They also often require blood thinners, which can increase the risk of bleeding. Xisomab 3G3 is type of drug called a monoclonal antibody that may prevent blood clots caused by a catheter in patients receiving chemotherapy.

NCT ID: NCT04400799 Terminated - COVID-19 Clinical Trials

Enoxaparin for Primary Thromboprophylaxis in Ambulatory Patients With COVID-19

Start date: June 15, 2020
Phase: Phase 3
Study type: Interventional

The OVID study will show whether prophylactic-dose enoxaparin improves survival and reduces unplanned hospitalizations in ambulatory patients aged 50 or older diagnosed with COVID-19, a novel viral disease characterized by severe systemic, pulmonary, and vessel inflammation and coagulation activation.

NCT ID: NCT04345848 Terminated - COVID Clinical Trials

Preventing COVID-19 Complications With Low- and High-dose Anticoagulation

COVID-HEP
Start date: April 28, 2020
Phase: Phase 3
Study type: Interventional

The ongoing COVID-19 pandemic affects millions of humans worldwide and has led to thousands of acute medical hospitalizations. There is evidence that hospitalized cases often suffer from an important infection-related coagulopathy and from elevated risks of thrombosis. Anticoagulants may have positive effects here, to reduce the burden of thrombotic disease and the hyperactivity of coagulation, and may also hold beneficial anti-inflammatory effects against sepsis and the development of ARDS. The investigators hypothesize that high-dose anticoagulants, compared with low-dose anticoagulants, lower the risk of venous and arterial thrombosis, disseminated intravascular coagulation (DIC) and mortality. This open-label controlled trial will randomize hospitalized adults with severe COVID-19 infection to therapeutic anticoagulation vs. thromboprophylaxis during the hospital stay.

NCT ID: NCT04128956 Terminated - Venous Thromboses Clinical Trials

Aspirin® Plus Rivaroxaban Versus Rivaroxaban Alone for the Prevention of Venous Stent Thrombosis in Patients With PTS

ARIVA
Start date: March 11, 2020
Phase: Phase 2
Study type: Interventional

To show if a combination therapy of rivaroxaban plus Aspirin® is more efficient (superiority testing) as rivaroxaban alone in the prevention of early venous stent thrombosis in patients suffering from post-thrombotic syndrome in the first 6 months following endovascular therapy To demonstrate tolerability of combination therapy of Aspirin® plus rivaroxaban in long-term treatment.