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Hemostatic Disorders clinical trials

View clinical trials related to Hemostatic Disorders.

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NCT ID: NCT05295693 Completed - Coagulopathy Clinical Trials

Quantra vs TEG for Congenital Cardiac Surgery - a Pilot Validation Study

Start date: October 13, 2022
Phase:
Study type: Observational

Congenital heart surgery on cardio-pulmonary bypass (CPB) is associated with impacted coagulation quality and increased bleeding after separation of CPB. The current testing device used at our institution is the "TEG 5000" (Haemonetics Corporation). The novel coagulation testing device "Quantra System" (Hemosonics) has favorable properties (result within 20 minutes) allowing for a quicker identification of the coagulation problem and hence faster administration of the correct coagulation products, potentially leading to better coagulation quality and possibly reducing the need of additional blood products. The aim of this prospective observational (non-interventional, investigational only) quality improvement study is to investigate if the Quantra is reliable and valid in predicting the coagulation status when compared with our standard-of-care device TEG 5000.

NCT ID: NCT05290675 Completed - Clinical trials for Coagulation Defect; Bleeding

Quantra QPlus Sample Type Comparison

Start date: November 4, 2021
Phase:
Study type: Observational

This is a single center prospective observational study to compare QPlus parameter measurements in arterial and venous blood samples collected in parallel from patients undergoing cardiac surgery.

NCT ID: NCT05272475 Completed - Clinical trials for Coagulation Disorder

The Acute Effects of Chamomile Intake on Blood Coagulation Tests in Healthy Volunteers

Start date: March 16, 2022
Phase: N/A
Study type: Interventional

Chamomile may possess anticoagulant effects based on the presence of coumarin-like compounds within the flower. This randomized complete crossover study will investigate the impact of chamomile ingestion acutely on coagulation.

NCT ID: NCT05237492 Completed - Drug Toxicity Clinical Trials

The Influence of Tramadol on Platelet Function

Start date: January 26, 2022
Phase: Phase 4
Study type: Interventional

The aim of this ex-vivo study is to quantify the effect of tramadol on platelet aggregation.

NCT ID: NCT05224388 Completed - COVID-19 Clinical Trials

Evaluating Dose Regimen of Intravenous Unfractionated Heparin and Low Molecular Weight Heparin in Critical Ill Patients Versus Critical Ill COVID-19 Patients Using Anti-Xa Levels.

Start date: January 1, 2020
Phase:
Study type: Observational

To see whether our increased dosing regimen of unfractionated heparin (UF) and low molecular weight heparin (LMWH) in COVID-19 patients was effective at preventing thrombo-embolic complications. We did regular anti-Xa tests to optimise the dose of our thromboprophylaxis. Furthermore, we want to examine the time it takes to reach adequate anti-Xa levels, to determine additional risk factors and do a subgroup analysis. Lastly, we will study if there are possible complications of our thromboprophylactic therapy.

NCT ID: NCT05214300 Completed - Bleeding Disorder Clinical Trials

Screening for Bleeding Disorders in Children

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

The investigators try to improve the screening of bleeding disorders in children by identifying symptoms, laboratory abnormalities and clinical scores discriminating patients congenital bleeding disorders in order to create a simple screening algorithm applicable in pediatrics, aiming for use in pre-anesthetic consultation and in consultation by pediatricians and general practitioners.

NCT ID: NCT05162339 Completed - Clinical trials for Inflammatory Bowel Diseases

Inflammatory Bowel Disease and Thromboembolic Events

Start date: November 1, 2016
Phase:
Study type: Observational [Patient Registry]

The main objective was to demonstrate the existence and importance of hypercoagulability in patients with IBD, by determining the prevalence of changes in coagulation parameters and evaluating the impact of these changes on the occurrence of thromboembolic events.

NCT ID: NCT05152420 Completed - Clinical trials for Coagulation Disorder

Study of Intravenous VMX-C001 in Healthy Subjects and in Combination With Selected Direct Oral Anticoagulants in Healthy Older Subjects

Start date: October 29, 2021
Phase: Phase 1
Study type: Interventional

A single centre, double-blind, randomized, parallel group, placebo-controlled study in healthy subjects conducted in two parts: Part 1: Single ascending doses in healthy subjects aged 18 to 49 years to assess safety, pharmacokinetics (PK) and pharmacodynamic (PD) effects of VMX-C001. Part 2: Healthy subjects aged 50 to 79 years to assess safety, PK and PD effects of VMX-C001 in the presence of DOACs.

NCT ID: NCT05137249 Completed - COVID-19 Clinical Trials

The Glycocalyx in COVID-19 Patients. A Pilot Study

Glycovid-19
Start date: December 1, 2020
Phase:
Study type: Observational

The damage of the endothelial glycocalyx is based on microvascular endothelial dysfunction and typical for critical clinical conditions like sepsis, trauma, bleeding, shock, as well as ARDS. We aim to generate first hints regarding the impact of covid-19 disease on the (damage) of the endothelial glycocalyx. Furthermore, we want to investigate the potential coagulopathies, which go along with shedding of the glycocalyx. The detection of and the relation between the severity of the disease, as well as the extent of the glycocalyx damage during the observational period, as well as the hemostatic alterations, are aim of the study.

NCT ID: NCT05064267 Completed - Clinical trials for Renal Insufficiency, Chronic

Hemostatic Profiles in Pediatric CKD

Start date: November 15, 2021
Phase:
Study type: Observational

This cross-sectional pilot study will examine the blood clotting patterns in children with chronic kidney disease stages 3, 4, and 5. A total of 30 participants will be enrolled with 10 participants for each stage of chronic kidney disease. Blood specimens will be collected from each participant during a routine clinic visit, and will then be processed to evaluate blood clotting characteristics according to thrombelastography and more conventional clotting tests.