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NCT ID: NCT02481206 Terminated - Clinical trials for Sudden Cardiac Death

Wearable Cardioverter Defibrillator in Hemodialysis Patients (WED-HED) Study

WED-HED
Start date: June 2015
Phase: N/A
Study type: Interventional

A multi-center, prospective, randomized controlled clinical trial with 1:1 assignment of treatment and control. This study will evaluate the impact of wearable cardioverter defibrillator use on sudden cardiac death in incident hemodialysis patients. The study will enroll up to 2,600 subjects. A maximum of 200 sites in the USA will be used for enrollment.

NCT ID: NCT02148055 Terminated - Clinical trials for Spontaneous Intra Uterine Fetal Death

Comparative Evaluation of IRM and Autopsy in the Evaluation of Intra Uterine Fetal Death

COMPER
Start date: May 2014
Phase: N/A
Study type: Interventional

Fetal intra uterine death is a rare event (incidence 2/1000 births) , unexpected and psychologically painful for the couple and the healthcare team. In this difficult context, it is essential to understand the etiology of death to guide the management of subsequent pregnancies. Among the investigations, foetopathologic examination is essential, but the examination of the brain is not possible in more than half of the cases due to the cerebral maceration due to the incompressible delay between death and expulsion. The use of MRI as a diagnostic tool fetal post- mortem " virtual autopsy " performed before expulsion of the fetus is interesting because it would permit to obtain a macroscopic examination of the fetal brain, archivable, and a gain concerning the diagnosis. Thus, a normal MRI will exclude cerebral anatomical abnormality , stroke or bleeding . If MRI abnormalities are found , it will not only guide the foetopathologic review, but mainly to guide the etiology . On the other hand , it is a non-invasive tool and acceptability by the couple would be better than autopsy which is often refused by the couple in this difficult psychological context. In this study , MRI will be given in addition to conventional autopsy in the painful waiting time between the time of diagnosis of death and expulsion without delaying care . If this study is validated , MRI may be systematically proposed in this indication or alternative to autopsy when it will be refused by the parents.

NCT ID: NCT01948206 Terminated - Clinical trials for Sudden Cardiac Death

Study of Paced QRS Duration as a Marker of Sudden Cardiac Death

Start date: October 2013
Phase: N/A
Study type: Observational

The purpose of the study is to determine whether prolonged paced QRS duration is a marker of sudden cardiac death in subjects with implantable cardioverter-defibrillators (ICD).

NCT ID: NCT01884129 Terminated - Recurrence Clinical Trials

Prognostic Value of CTC in HNSCC Patients

CTCHNSCC01
Start date: June 2012
Phase: N/A
Study type: Observational [Patient Registry]

We hypothesized that the number of circulating tumor cells (CTCs) and molecular markers on CTCs could be a prognostic factor or predictive factor to patients with head neck cancer.

NCT ID: NCT01810640 Terminated - Liver Disease Clinical Trials

Pre-recovery Bedside Liver Biopsy in Brain Death Organ Donors

PPB
Start date: February 2013
Phase: N/A
Study type: Interventional

This study's objective is to obtain preliminary data to test the hypotheses that percutaneous liver biopsy in brain death donors is safe and provides reliable histological information. Furthermore, that information when disseminated fully and widely many hours before organ recovery would not only decrease economic costs of wasteful recovery of livers that are not ultimately transplanted but also increase transplantation and decrease cold ischemia times of recovered livers.

NCT ID: NCT01448005 Terminated - Myocardial Ischemia Clinical Trials

LifeVest Post-CABG Registry

Start date: February 2011
Phase: N/A
Study type: Observational

This is a multi-center prospective registry of patients with an ejection fraction (EF) ≤ 35% following coronary artery bypass graft (CABG) surgery in order to test the hypothesis that wearable defibrillators (WD) will decrease overall mortality after discharge by decreasing arrhythmic death in this select population with high risk for sudden cardiac death (SCD). This is a pilot project to determine the feasibility of a larger-scale study.

NCT ID: NCT01393431 Terminated - Clinical trials for Ventilator Associated Pneumonia

Futility of Exhaled Breath Condensate pH Measurements in Ventilated Patients in Intensive Care Unit (ICU)

Start date: August 2007
Phase: N/A
Study type: Observational

Measurement of pH in Exhaled breath condensate has been mentioned as a robust variable from lung inflammation. It is non-invasive and reproducible. The investigators measured pH in the water condensed in the trap of expiratory arm of ventilator.In ICU the investigators measured pH in condensed water without interfering with patients treatment. A group of critically ill patients mechanically ventilated due to non pulmonary cause were followed until successful weaning, death or pneumonia. The investigators found that pH did not change along the study and it did not predict worsening condition.

NCT ID: NCT01321918 Terminated - Clinical trials for Extra-hospital Sudden Death

Register and DNA Bank of Adult Extra-hospital Sudden Death (Protocol FASTER)

Start date: June 2007
Phase: N/A
Study type: Interventional

The main objective of this study is the formation of a DNA bank to realise a case-control genetic study designed to identify sequence variations in DNA that predispose to sudden cardiac death in adults. The secondary objective of this study is the creation of a register for epidemiological surveillance of adult extra-hospital sudden death.

NCT ID: NCT00727363 Terminated - Death Clinical Trials

Prophylactic Probiotics in Premature Infants

C3P
Start date: August 2008
Phase: Phase 3
Study type: Interventional

This study tries to determine whether the oral administration of a specific probiotic (good bacteria) in premature infants hospitalized in a neonatal intensive care unit may prevent infections and the development of a severe inflammatory disease of the bowel called necrotizing enterocolitis. The investigators propose that premature infants not given probiotics will colonize their gut with bad bacterias and develop infection.

NCT ID: NCT00487279 Terminated - Clinical trials for Coronary Artery Disease

DEfibrillators To REduce Risk by MagnetIc ResoNance Imaging Evaluation

DETERMINE
Start date: June 2007
Phase: N/A
Study type: Interventional

This trial is a prospective, multi-center, randomized study of patients with coronary artery disease (CAD) and mild to moderate left ventricular (LV) dysfunction. The primary objective of this study is to test the hypothesis that Implantable Cardioverter Defibrillator (ICD) therapy in combination with medical therapy in patients with an infarct size greater than or equal to 10% of the left ventricular mass improves long term survival compared to medical therapy alone. In addition to the 2-arm randomized trial, the study will also include a non-investigational registry of non-randomized patients.