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Endocarditis, Bacterial clinical trials

View clinical trials related to Endocarditis, Bacterial.

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NCT ID: NCT05183555 Not yet recruiting - Clinical trials for Infective Endocarditis

Early Feasibility Study of Somatostatin Receptors PET Imaging for the Diagnosis of Infective Endocarditis

DOTENDO
Start date: April 2022
Phase: Phase 2
Study type: Interventional

Study hypothesis: 68Ga-DOTATOC PET/CT could detect cardiac foci of infective endocarditis regardless of the type of valve (native or prosthetic) and also extracardiac localizations related to this pathology (infection responsible, peripheral emboli, ...). This study is a proof of concept with low population

NCT ID: NCT05152225 Not yet recruiting - Clinical trials for Endocarditis, Bacterial

Neurological Complication of Infective Endocarditis: A Prospective Multi-site Cohort Study

Start date: January 1, 2022
Phase:
Study type: Observational [Patient Registry]

The main objective of this study is to better estimate the rate of infectious intracranial aneurysms (IIA) in proved infective endocarditis (IE). It also aims to identify MRI markers capable of accurately predicting (or excluding) IIA; to assess the impact of the different MRI abnormalities on the outcome; to capture the real-world management of EI with neurological complications in comprehensive IE centers in France

NCT ID: NCT05061355 Recruiting - Clinical trials for Endocarditis Infective

Antibiotics vs Antibiotics and Surgical ThERapy for Infective Endocarditis

ASTERIx
Start date: September 9, 2021
Phase: N/A
Study type: Interventional

Infective endocarditis (IE) is a deadly disease and the incidence is increasing. An important initial assessment of patients with IE includes whether surgical treatment is indicated; yet, appropriate data to guide this assessment do not exist. The ASTERIx study will assess whether a surgical approach in addition to medical care for treatment of IE is superior to medical care alone. In total, 496 patients will be included in the study over four years. The study is event-driven and will require at least 240 events. The study will assess the primary composite outcome of death, embolization, relapse of IE, new heart failure or reinfection. Study participants who survive to discharge will be followed by routine clinical check-ups at one- and four-weeks post-discharge and at three months. Additionally a 12-month study follow-up is planned. The investigators will also conduct a small substudy to assess the frequency of silent emboli.

NCT ID: NCT05037474 Active, not recruiting - ICD Clinical Trials

Contemporary Transvenous Lead Extraction Outcomes

TLE
Start date: April 1, 2020
Phase:
Study type: Observational

Presentation of procedural safety and outcomes data from a high volume TLE centre

NCT ID: NCT04992923 Recruiting - Clinical trials for Infective Endocarditis

Prospective Cohort Study of Patients With Infective Endocarditis at Pitié-Salpêtrière Hospital

EIPSL
Start date: September 15, 2020
Phase:
Study type: Observational [Patient Registry]

Infective endocarditis (IE) is a severe condition associated with high mortality. Due to the relative low prevalence of IE, prospective data are lacking and current guidelines are mostly based on expert consensus with low level of evidence. IE is also associated with severe complications especially strokes that occur in about one third of the patients. In order to improve the management and the prognosis of IE, clinical data from larges prospective cohort studies are needed.

NCT ID: NCT04977518 Completed - Clinical trials for Infective Endocarditis

Characteristics of Infective Endocarditis in East China

Start date: January 1, 2008
Phase:
Study type: Observational

This was a retrospective observational study of consecutive cases of definite or possible infective endocarditis (IE) as per the modified Duke criteria between January 2008 and December 2015, which was performed at the Second Affiliated Hospital of Zhejiang University, School of medicine (SAHZU), a tertiary care referral hospital located in East China.

NCT ID: NCT04840225 Recruiting - Anemia Clinical Trials

Anemia in Patients With Endocarditis

ANIE
Start date: March 22, 2021
Phase:
Study type: Observational

Prospective study of prevalence and deep charecterization of anemia in patients with endocarditis from diagnosis undtill 6 months after discharge.

NCT ID: NCT04838938 Completed - Treatment Clinical Trials

Personalized Medicine in Patients With Infective Endocarditis

Start date: March 1, 2021
Phase:
Study type: Observational [Patient Registry]

The hypothesis underlying this work is the identification of different sub phenotypes of patients with infective endocarditis through the study of the host's response to infection. Furthemore, metagenomic sequencing may be a helpful supplement to IE diagnostic, especially when conventional tests fail to yield a diagnosis.

NCT ID: NCT04792281 Recruiting - Clinical trials for Infective Endocarditis

Impact of FDG-PET/CT on Management of Patients With Native Valve Infective Endocarditis

PET-NAVIE
Start date: August 31, 2021
Phase:
Study type: Observational

The proposed study is a multicentric prospective observational cohort study of patients with suspected NVE. The study population includes those with Possible IE according to the modified Duke criteria and investigated at one of the 6 participating sites which include 2 cardiac centers, the MHI and the IUCPQ, as well as 4 tertiary care centers, the Jewish General Hospital , the McGill University Health Centre and the CHUS.

NCT ID: NCT04647331 Recruiting - Clinical trials for Infective Endocarditis

Betalactam Pharmacokinetics in Endocarditis Patients

Start date: June 1, 2021
Phase:
Study type: Observational

Infectious endocarditis (IE) is associated with mortality rates of 10-12%. Adequate antibiotic therapy is crucial for survival and is administered in high doses due to the severity of the disease. In most cases, beta-lactam antibiotics (e.g. ampicillin, penicillin G, cefotaxime or cloxacillin) are employed. A number of patient characteristics, such as age, body weight, and renal function) influence the pharmacokinetics of these drugs. Yet, the interindividual variability is poorly understood meaning that a large proportion of patients are at risk of subtherapeutic or excessive drug concentrations that might result in treatment failure or side effects, respectively. In the present study, data will be collected on antibiotic concentrations in patients treated with beta-lactams for infectious endocarditis as well as patient characteristics and treatment outcomes. A mathematical model will be developed to determine which patient factors determine drug pharmacokinetics. Based on this model, predictions will be made by mathematical simulations on which dosing regimens are optimal for individual patients to ensure therapeutic and non-toxic drug concentrations. In total, 150 patients will be included at four University Hospitals in Sweden; Uppsala University Hospital, Sahlgrenska University Hospital in Gothenburg, Skåne University Hospital in Lund and Karolinska University Hospital in Stockholm. Following informed consent to participate blood samples will be collected at 6 time-points during a dose interval and then at 3 time-points weekly during the full treatment episode (maximum 6 weeks).