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Platelet Dysfunction clinical trials

View clinical trials related to Platelet Dysfunction.

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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: NCT05033236 Completed - Clinical trials for Inflammatory Response

Platelets and Complement Activation in Coronary Artery Bypass Graft Surgery (CABG)

PAC
Start date: November 23, 2018
Phase:
Study type: Observational [Patient Registry]

Patients undergoing coronary artery bypass graft surgery (CABG) frequently exhibit postoperative bleeding complications which are still a major cause for morbidity and mortality. One major contributing factor is the loss of platelets and impaired platelet function. During cardiopulmonary bypass (CPB) blood comes in close contact with foreign surfaces which induces a series of reactions; especially the complement system as part of the innate immunity is highly activated. Due to the strong crosslink between complement system, platelet function and the plasmatic coagulation it is likely that complement activation during CPB has an impact on the overall process of clot formation. Besides the activation of the complement system there is growing evidence that the occurrence of mitochondrial DNA (mtDNA) during CPB might be related to further platelet activation . Activated platelets may enhance micro-thrombosis leading to organ failure and thereby contributing to postoperative morbidity. One major complication during and after CABG surgery is bleeding requiring transfusion and even reoperation in about 2%- 8% of patients. As bleeding complications increase patient morbidity and mortality, this study is designed to investigate the possible mechanisms of platelet loss during CABG. The hypothesis is that increased complement activation during CPB leads to platelet activation and loss of platelets. Further the degree of complement activation and levels of mtDNA might correlate with postoperative bleeding, transfusion requirements and clinical outcome.

NCT ID: NCT04734028 Completed - Clinical trials for Coronary Artery Disease

PTRG-DES Consortium

PTRG
Start date: July 9, 2003
Phase:
Study type: Observational

The PTRG-DES consortium is a coalition composed of multi-center, real-world registries including CAD patients treated with DES in South Korea. From 9 academic registries in Korea, a total of 13,160 patients were enrolled for this database between July 2003 and August 2018. The aim of the study was to investigate long-term prognostic implications of platelet function and genotypes after DES implantation for significant CAD in South Korea.

NCT ID: NCT04554901 Completed - Clinical trials for Platelet Dysfunction

The Effect of Cocoa on Platelet Function Profiles in Patients

ECLAIR
Start date: September 1, 2020
Phase: N/A
Study type: Interventional

The effects of chocolate on cardiovascular health are still a matter of debate. It can potentially favor cardiovascular health through the antioxidative effects of cocoa ingredients, such as polyphenols (present in dark but not white chocolate).

NCT ID: NCT04400760 Completed - Clinical trials for Platelet Dysfunction

The Effect of Dapagliflozin on Platelet Function testinG Profiles in Diabetic PatiEnts.

EDGE
Start date: May 1, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

Sodium GLucose Transport 2 inhibitors (SGLT2I), including dapagliflozin, reduce the likelihood of hospitalization for heart failure and death in persons with type 2 diabetes, of which the mechanism has not been fully elucidated. The mechanistic effects of dapagliflozin on platelet function profiles have not yet been ascertained. It remains unclear if this reduction in cardiovascular death is mediated by decreased platelet reactivity.

NCT ID: NCT03667066 Completed - Clinical trials for Platelet Dysfunction

clOpidogrel "resIstaNce" in a Selected Population of Patients at a Tertiary Cardiovascular Center in Trinidad

POINT
Start date: September 1, 2017
Phase:
Study type: Observational

The aim of this study was to determine the prevalence of clopidogrel resistance among a selected group of patients undergoing elective percutaneous coronary intervention and to observe whether there was any south-Asian (Indo-Trinidadian) predilection for HPR considering the well-established epidemiologic trends for accelerated CAD within this subgroup.

NCT ID: NCT03621020 Completed - Healthy Clinical Trials

Clinical Performance Evaluation of T-TAS 01 PL Chip

Start date: September 1, 2018
Phase:
Study type: Observational

This study will measure primary hemostatic ability using the T-TAS 01 System with PL chip, with a comparison to clinical truth.

NCT ID: NCT03458351 Completed - Clinical trials for Platelet Dysfunction

RIPC and Platelet Activation on Platelet Activation During Cardiopulmonary Bypass

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

In this study, the investigators are going to investigate the effects of remote ischemic preconditioning on platelet activation in patients undergoing cardiac surgery with cardiopulmonary bypass.

NCT ID: NCT03455218 Completed - Inflammation Clinical Trials

Nitric Oxide Administration During Pediatric Cardiopulmonary Bypass Surgery to Prevent Platelet Activation

Start date: April 25, 2018
Phase: Phase 2/Phase 3
Study type: Interventional

Open heart surgery requires the use of a cardiopulmonary bypass (CPB) circuit. As blood flows across the artificial surfaces of the CPB circuit, platelets are activated and consumed. This activation results in a profound inflammatory reaction and need for transfusion. This reaction is intensified in younger, smaller patients undergoing longer, more complex open heart surgery. Nitric oxide is naturally released by vascular endothelial surfaces and acts as a signaling molecule which prevents platelet activation. The investigators hypothesize that the addition of the nitric oxide to the sweep gas of the oxygenator during cardiopulmonary bypass surgery will replace this natural endothelial function and thus prevent platelet activation and consumption. The investigators plan to test this hypothesis with a pilot double blinded, randomized trial of 40 patients less than a year of age undergoing cardiac surgery requiring CPB.

NCT ID: NCT03188705 Completed - Clinical trials for Coronary Artery Disease

CES1 Carriers in the PAPI Study

Start date: October 14, 2019
Phase: Phase 4
Study type: Interventional

This study builds, in part, upon preliminary results generated as part of the Pharmacogenomics Anti-Platelet Intervention (PAPI) Study (NCT00799396). The purpose of this investigation is to assess the impact of genetic variation in the carboxylesterase 1 (CES1) on response to clopidogrel as well as dual antiplatelet therapy (i.e. clopidogrel and aspirin), as assessed by ex vivo platelet aggregometry, in healthy Amish individuals. The investigators hypothesize that participants who carry alleles that modify the activity or expression of CES1 will have altered response to clopidogrel as well as dual antiplatelet therapy.