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Hemostasis clinical trials

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NCT ID: NCT04377490 Recruiting - COVID-19 Clinical Trials

Thrombo Embolic Events in Hospitalized Patients With Covid-19 Serious Acute Pneumopathy

THROMBCOVID2
Start date: May 4, 2020
Phase:
Study type: Observational

The understanding of haemostasis and inflammation cross-talk has gained considerable knowledge during the past decade in the field of arterial and venous thrombosis. Complex and delicately balanced interaction between coagulation and inflammation involve all cellular and humoral components. Elements of the coagulation system such as activated thrombin, fibrinogen or factor Xa may increase inflammation by promoting the production of proinflammatory cytokines, chemokines, growth factors and adhesion molecules that lead to a procoagulant state amplifying the pathological process. Recent evidence supports inflammation as a common pathogenic contributor to both arterial and venous thrombosis, giving rise to the concept of inflammation induced thrombosis. Patients with infection of COVID-19 and severe pneumoniae seem to have higher risk of thromboembolism. The purpose of this project is to analyze hemostasis and coagulation of every hospitalized patient with infection of COVID-19. Blood sample for coagulation and hemostasis analysis will be collected on every patient hospitalized in Amiens hospital for COVID-19 infection. Thrombin time, factors V and II, fibrin/fibrinogen degradation products, antithrombin will be assessed every week. Anticardiolipin, anti-beta2 glycoprotein I and anti-annexin A2 antibodies IgG and IgM at day of admission and at fourth week after admission will be assessed. SARS-CoV2 viral load and serodiagnosis will be performed at the same time. At the same time venous ultrasound to diagnose thrombosis will be performed.

NCT ID: NCT04366752 Completed - COVID-19 Clinical Trials

Thrombo Embolic Events in Critical Care Patients With Covid-19 Serious Acute Pneumopathy

THROMBOCOVID
Start date: April 22, 2020
Phase:
Study type: Observational

The understanding of haemostasis and inflammation cross-talk has gained considerable knowledge during the past decade in the field of arterial and venous thrombosis. Complex and delicately balanced interaction between coagulation and inflammation involve all cellular and humoral components. Elements of the coagulation system such as activated thrombin, fibrinogen or factor Xa may increase inflammation by promoting the production of pro-inflammatory cytokines, chemokines, growth factors and adhesion molecules that lead to a procoagulant state amplifying the pathological process. Recent evidence supports inflammation as a common pathogenic contributor to both arterial and venous thrombosis, giving rise to the concept of inflammation-induced thrombosis. Patients with infection of COVID-19 and severe pneumoniae seem to have higher risk of thromboembolism. Very few data are available regarding the biological disorders of coagulation in these patients. Th purpose of this project is to analyze hemostasis and coagulation of patients with infection of COVID-19 and severe pneumonia.

NCT ID: NCT04268992 Completed - Clinical trials for Coronary Artery Disease

Effect of Long-term Exercise on Haemostasis and Inflammation in Patients With Coronary Artery Disease

Start date: July 3, 2020
Phase: N/A
Study type: Interventional

Introduction: Regular exercise training improves prognosis in patients with coronary artery disease (CAD). This study investigates whether the beneficial effects of exercise can be partly explained by favourable changes in haemostasis and inflammation. Methods: 150 CAD patients are randomised to a supervised long-term exercise program (3 months) or usual care. Blood samples are obtained at baseline, 1.5 months, and 3 months after randomisation. Results: The investigators will evaluate platelet turnover and aggregation, coagulation, fibrinolysis, and inflammatory markers before and after short- and long-term exercise, and the two randomised groups will be compared. Perspectives: The present study will increase our knowledge of the beneficial mechanisms underlying the effect of exercise in CAD patients, potentially paving the way for improved exercise recommendations.

NCT ID: NCT03932240 Completed - Hemostasis Clinical Trials

In Vivo Effects of Fibrinogen Concentrate (FC) Versus Cryoprecipitate on the Neonatal Fibrin Network Structure After Cardiopulmonary Bypass (CPB)

Start date: August 13, 2019
Phase: Phase 3
Study type: Interventional

This primary aim of this study is to compare the in vivo effects of fibrinogen concentrate and cryoprecipitate on the neonatal fibrin network after surgery with cardiopulmonary bypass to develop effective and safe strategies for managing coagulopathies in neonates.

NCT ID: NCT03907111 Completed - Hemostasis Clinical Trials

Compare the Hemostatic Effectiveness of Chitosan Gauze With Traditional Gauze on Open Wound on 10 Participants.

Start date: October 2, 2015
Phase: N/A
Study type: Interventional

This study recruited 10 subject participants to compare the hemostasis gauze made by chitosan with traditional cotton gauze to see which one is better in bleeding time, bleeding volume, wound infection and wound healing speed when it is used in open wound treatment.

NCT ID: NCT03896061 Completed - Hemostasis Clinical Trials

A Videographic Study to Evaluate the Impact of a Pulsed Firing Technique on Staple Line Interventions in Laparoscopic Sleeve Gastrectomy

Start date: April 15, 2019
Phase:
Study type: Observational

Prospective, multi-center study will evaluate a pulsing technique with the ECHELON FLEX GST system for hemostasis at the staple line in laparoscopic sleeve gastrectomy procedures.

NCT ID: NCT03873181 Completed - Hemostasis Clinical Trials

Post-Market Evaluation of HEMOBLASTâ„¢ Bellows in Laparoscopic Abdominal, Gynecological, and Urological Surgery

NOBLE-Laparo
Start date: May 16, 2019
Phase:
Study type: Observational

A prospective, multi-center, multi-national single arm study to evaluate the performance and safety of HEMOBLASTâ„¢ Bellows in laparoscopic abdominal, gynecological, and urological surgery.

NCT ID: NCT03873168 Terminated - Hemostasis Clinical Trials

Post-Market Evaluation of HEMOBLASTâ„¢ Bellows in Open Gynecological, Urological, ENT, Head, Neck, and Vascular Surgeries

NOBLE-Open
Start date: May 9, 2019
Phase:
Study type: Observational

A prospective, multi-center, multi-national single arm study to evaluate the performance and safety of HEMOBLASTâ„¢ Bellows in open gynecological, urological, ENT and head and neck, and vascular surgery.

NCT ID: NCT03711916 Completed - Breast Cancer Clinical Trials

Post-Operative Outcomes of Low Thermal Dissection vs. Traditional Electrosurgery

Start date: March 17, 2017
Phase: N/A
Study type: Interventional

Low thermal dissection devices have been introduced as a tool to improve surgical outcomes. PlasmaBlade, a low thermal dissection device, has shown to be associated with effective cutting, and significantly lower temperature than traditional electrosurgical dissection device. Thus, low thermal devices would improve flap perfusion by decreasing the thermal injury resulted by the dissection. Looking into the use of low thermal devices in cases of mastectomy and immediate breast reconstruction has not been documented. The aim of this study is to determine if there are clinical flap perfusion, surgical site drainage, and pain scores differences between mastectomy flaps created using low thermal dissection device and those done with the standard care of Bovie cautery in order to warrant a formal study.

NCT ID: NCT03654560 Completed - Bleeding Clinical Trials

Efficacy and Safety of HemoStyp as an Adjunct for Management of Secondary Hemostasis in the Operative Setting

Start date: December 28, 2018
Phase: N/A
Study type: Interventional

The purpose of the study is to assess efficacy and safety of HemoStyp as an adjunct for management of secondary hemostasis in the operative setting.