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Biomarkers clinical trials

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NCT ID: NCT05095324 Active, not recruiting - Sepsis Clinical Trials

The Biomarker Prediction Model of Septic Risk in Infected Patients

Start date: September 7, 2021
Phase:
Study type: Observational [Patient Registry]

Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to an infection. Sepsis is associated with high mortality because of the complex mechanisms. In China, the mortality of sepsis in ICU was up to 35.5%. As a major and urgent global public health challengeļ¼Œsepsis is hard to treat because of the complexion and highly heterogeneous in clinical manifestation. The early diagnosis and stratification of the infection is very important. If we can identify the patients who may developed into the sepsis, the therapeutic regimen was not only antibiotic, but also included stable the vascular endothelial cellsļ¼Œregulation of coagulation function and protection of organ functions. Biomarkers have an important place in sepsis because they are strictly related to the organ damage. Each organ has its own specific biomarkers, and these biomarkers will change according to the severity of the disease. So the investigators want to find the difference of biomarkers of each organ in patients from infection to spesis.

NCT ID: NCT03962361 Active, not recruiting - Biomarkers Clinical Trials

New Biomarkers of Neurological Outcome After a Sudden Cardiac Death

Start date: February 2016
Phase:
Study type: Observational

The aim of the project is to establish the value of circulating microparticles as a new biomarker for neurological prognosis of patients recovered from sudden cardiac death who remain comatose.

NCT ID: NCT03926572 Active, not recruiting - Clinical trials for Hypertension, Pulmonary

Acute Decompensation of Pulmonary Hypertension

PROPULS
Start date: September 19, 2019
Phase: N/A
Study type: Interventional

The main objective of this study is to analyze the survival of a cohort of patients admitted for acute decompensation of pulmonary arterial hypertension or postembolic pulmonary hypertension and to establish the prognostic value of biomarkers.

NCT ID: NCT03735719 Active, not recruiting - Heart Failure Clinical Trials

Biomarkers for Risk Stratification After STEMI

Start date: April 2014
Phase:
Study type: Observational

Despite modern reperfusion strategies, myocardial infarction leads to deleterious processes resulting in left ventricular remodelling (LVR) and heart failure (HF). Several biomarkers i.e. galectin-3 (Gal-3) and soluble ST-2 protein are involved in LVR as a result of inflammatory processes and fibrosis. There is an evidence of a high prognostic value of both biomarkers in prediction of outcomes in HF patients. This study will further investigate the role of Gal-3 and ST-2 in patients with ST-segment elevation myocardial infarction (STEMI) treated with primary percutaneous coronary intervention (PCI) and without prior HF in prediction of unfavourable outcomes.

NCT ID: NCT03263039 Active, not recruiting - Biomarkers Clinical Trials

Biomarkers in Urothelial Cancer Patients Treated With Pembrolizumab

RESPONDER
Start date: August 21, 2017
Phase: Phase 2
Study type: Interventional

In the RESPONDER study, the role of the immune evasive mechanisms combined with genomic characterization will be explored in urothelial cancer patients treated with second-line treatment with pembrolizumab. Combined profiling of immune and molecular status is novel and may contribute to improved patient stratification and provide rationale for future treatment strategies containing pembrolizumab.

NCT ID: NCT02732301 Active, not recruiting - Clinical trials for Cardiopulmonary Bypass

Postoperative Gastrointestinal Dysfunction After Cardiac Surgery - Occurrence and Search for Biomarkers

GAINDYSFUNCS
Start date: November 2015
Phase:
Study type: Observational

The purpose of this study is to investigate the frequency and grade of gastrointestinal dysfunction in patients after thoracic cardiovascular surgery, and to search for biomarkers of gastrointestinal dysfunction. All adult patients undergoing elective cardiac surgery requiring cardiopulmonary bypass at Örebro University Hospital, Örebro, Sweden, are asked for participation in this study. All participating patients sign informed consent at the inclusion. The first three postoperative days the function of the gastrointestinal tract is scored according to a rating scale (grade 0-4), along with other clinical parameters. Plasma blood samples are collected from each patient preoperatively and the first three postoperative days. The plasma samples are stored in a biobank for later determination of plasma proteins. In the analysis, the patients are divided according to the gastrointestinal rating scale and the plasma protein expression, gastrointestinal complications and all-cause mortality are compared between the groups.