Clinical Trials Logo

Thrombosis clinical trials

View clinical trials related to Thrombosis.

Filter by:

NCT ID: NCT04330170 Completed - Clinical trials for Deep Vein Thrombosis, Pulmonary Embolus

Inferior Vena Cava Filters: Analysis of a Database

Start date: January 13, 2016
Phase:
Study type: Observational

In this study a retrospective analysis of patients database was performed, who underwent treatment for deep vein thrombosis in tertiary hospital by using inferior vena cava-filters

NCT ID: NCT04305756 Completed - Thrombosis Clinical Trials

Impact of Prophylactic Low-molecular Weight Heparin Dosing on Clotting Parameters Following Cesarean Delivery

Start date: June 12, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the efficacy of two dosing regimens of low molecular weight heparin (LMWH) to reach prophylactic anti-factor Xa levels in post-cesarean delivery women. Half of participants will receive a fixed dose of LMWH, while the other half will receive a weight-based dose. The hypothesis is that the use of a weight-based dose will result in more women reaching prophylactic levels.

NCT ID: NCT04302376 Completed - Clinical trials for Central Venous Catheter Thrombosis

Thrombotic Complications After Central Venous Catheterization

TARZAN
Start date: December 1, 2019
Phase:
Study type: Observational

Rationale: Complications related to central venous catheterization are mechanical, infectious or thrombotic in origin. Potential complications of catheter-related thrombosis are not insubstantial and include pulmonary embolism, post-thrombotic syndrome or thrombophlebitis. Prevalence and incidence of catheter-related thrombosis at the intensive care unit is unclear and treatment, especially of asymptomatic thrombosis, remains ambiguous. Therefore a study is warranted that evaluates the prevalence and incidence of catheter-related thrombosis and investigates its potential consequences. We hypothesize that the incidence of catheter-related thrombosis is 5-15%. Objective: To assess the prevalence and incidence of symptomatic and asymptomatic catheter-related thrombosis.

NCT ID: NCT04297787 Completed - Clinical trials for Acute Deep Vein Thrombosis

Safety and Efficacy of Thrombolysis in Combination With Endhole Aspiration in the Treatment of Acute DVT

INDIGO
Start date: September 23, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate the safety and efficacy of thrombolysis in combination with endhole aspiration in the treatment of acute deep vein thrombosis (DVT). Secondarily, the study team hope to illuminate the financial implications of single session catheter directed therapy versus a potential 48 hour lysis procedure (Lysis is an approach in which vascular specialists deliver clot-dissolving drugs directly to the site of the clot through a catheter).

NCT ID: NCT04272723 Completed - Pulmonary Embolism Clinical Trials

Management of Venous Thromboembolism in France: a National Survey Among Vascular Medicine Physicians

Observ-MTEV
Start date: August 21, 2019
Phase:
Study type: Observational

In France, venous thromboembolic (VTE) disease is usually managed by vascular medicine physicians (VMP). The national OPTIMEV study, conducted more than 12 years ago among VMP practicing in hospital and in the community described the management of VTE in routine clinical practice. Since then a large number of practice changing studies have been published. This includes trials that have validated the use of direct oral anticoagulants (DOAC), the new standard of care of VTE, as per new national and international guidelines. Management of VTE in 2019 appears to be significantly different from the one that prevailed more than 10 years ago when the last national survey was conducted. It is therefore important to have an update on the routine clinical practice management of VTE by VMP. In this perspective the investigators aim to conduct a national survey among VMP practicing in France

NCT ID: NCT04229433 Completed - Thrombus Clinical Trials

The Multiple Dose of PK/PD Study of SHR2285 Tablets in Healthy Subjects

Start date: August 11, 2020
Phase: Phase 1
Study type: Interventional

The study is a randomized, single-blind, placebo-controlled, multiple-dose escalation Phase I trials. 2 dose groups were designed, 12 subjects in each dose group.The drug was administered single dose and multiple doses.

NCT ID: NCT04211584 Completed - Artery; Thrombosis Clinical Trials

The TENDERA Multicenter Clinical Trial

TDR
Start date: December 18, 2017
Phase: N/A
Study type: Interventional

TENDERA is a multicenter randomized controlled trial to compare traditional entry point in the radial artery for TRI and distal puncture at the anatomical snuffbox area for transradial Interventions. The Investigators hypothesized that novel entry point in radial artery may lessen vascular access site complication rate and especially the radial artery late occlusion rate.

NCT ID: NCT04196049 Completed - Clinical trials for Age-Related Macular Degeneration

Removal of Massive Subretinal Organized Blood Clot With Fragmatome

Start date: January 7, 2019
Phase:
Study type: Observational

By using the ultrasound power delivered by fragmatome, the hard, organized blood clot could be removed easily.

NCT ID: NCT04194736 Completed - Clinical trials for Central Venous Catheters

Evaluation of the Occurrence of Early Thrombosis on Central Venous Catheter by Ultrasound in Pediatric Intensive Care Unit

Thromb-US
Start date: June 10, 2021
Phase: N/A
Study type: Interventional

The objective of this study is to prospectively describe the incidence of early venous thrombosis secondary to the placement of a percutaneous central venous catheter, in a pediatric intensive care unit, by systematic ultrasound screening.

NCT ID: NCT04177576 Completed - Clinical trials for Myeloproliferative Neoplasm

Evaluation of New Biomarkers of Thrombosis in Myeloproliferative Neoplasms

MPN-BIOCLOT
Start date: February 24, 2020
Phase:
Study type: Observational

Thrombosis is the main cause of morbidity and mortality in patients with myeloproliferative neoplasms (MPN). However, the pathogenesis of thrombosis in MPN is still largely elusive. Neutrophils can release their decondensed chromatin as a network of extracellular fibers named NET for "neutrophils extracellular trap". NETs are known to be procoagulant. Our main objective is to quantify NETs biomarkers expression in MPN patients and define if they could be used as prognostic factors in the outcome of thrombosis in these patients.