Clinical Trials Logo

Death clinical trials

View clinical trials related to Death.

Filter by:

NCT ID: NCT02951871 Completed - Clinical trials for This Study Describes the Different Causes of Death in 237 FL Patients

Causes of Death in Follicular Lymphoma: a Single Center Retrospective Analysis

Start date: January 2000
Phase: N/A
Study type: Observational

Background.Although the life expectancy of patients with FL has recently increased, notably since the introduction of rituximab in combination with chemotherapy, little is known regarding the precise causes of patients death. Patients and methods'. This study describes the different causes of death in FL patients among followed since 2000 at Lyon University Hospital, centre Léon Bérard and Mayo Clinic. The causes of death will be classified as related to lymphoma progression, treatment-related toxicity (including TRM and secondary myelodysplastic syndrome/acute myeloid leukemia), secondary neoplasias, or other.

NCT ID: NCT02936869 Completed - Neonatal Death Clinical Trials

Incentives for Postnatal Care Demand

Start date: August 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to identify the causal impact of performance-based monetary incentives in increasing postnatal care (PNC) referrals by traditional birth attendants (TBAs), via a randomized controlled trial (RCT).

NCT ID: NCT02923726 Completed - Clinical trials for Sudden Cardiac Death

Assessment of Primary Prevention Patients Receiving An ICD - Systematic Evaluation of ATP

APPRAISE ATP
Start date: September 30, 2016
Phase: N/A
Study type: Interventional

The primary objective is to understand the role of antitachycardia pacing (ATP) in primary prevention patients indicated for ICD therapy and programmed according to current guidance of higher rate cut-offs and therapy delays. The time to first all-cause shock will be tested in subjects with standard therapy (ATP and shocks) compared to subjects programmed to shock only to assess equivalency.

NCT ID: NCT02902783 Completed - Critical Care Clinical Trials

DONATE-Pilot Study on ICU Management of Deceased Organ Donors

DONATE-Pilot
Start date: September 2015
Phase:
Study type: Observational [Patient Registry]

The DONATE-Pilot is a prospective observational cohort study in organ donation (OD) that observes the ICU management of consented deceased organ donors at 4 high volume centres over a period of 12 months each. The pilot study will be followed by a 1-year prospective national observational study a 15-20 ICUs across Canada.

NCT ID: NCT02894580 Completed - Clinical trials for Chronic Heart Failure

Primary Prevention of Sudden Cardiac Death (PREV-DEATH)

PREV-DEATH
Start date: January 2015
Phase: N/A
Study type: Observational

The efficacy of implantable cardioverter-defibrillators (ICD) in primary prevention of sudden cardiac death (SCD) is well demonstrated but pivotal studies have been published more than 10 years ago and implantation's conditions tend to change.

NCT ID: NCT02848781 Completed - Clinical trials for Ventricular Tachycardia (VT)

Pan-Asia United States PrEvention of Sudden Cardiac Death Catheter Ablation Trial

PAUSE-SCD
Start date: November 30, 2015
Phase: N/A
Study type: Interventional

The current standard of care for ventricular tachycardia (VT) includes the use of medicine called anti-arrhythmic drugs (AADs) and Implantable Cardioverter Defibrillator (ICD) therapy. These treatments are used to terminate the irregular heartbeats and bring the heart back to a normal rhythm. Catheter ablation is a procedure used to eliminate (damage) the heart cells causing the arrhythmia. Patients eligible for this may benefit from an ablation procedure in addition to an ICD to treat their VT condition or risk of developing VT. This study aims to show that treating VT with catheter ablation, if performed preemptively at the time of ICD implantation, will reduce subsequent recurrent VT, ICD shocks, and lead to improved survival.

NCT ID: NCT02828137 Completed - Clinical trials for Myocardial Infarction

Relation Between NLR and IMR in STEMI Patients

Start date: May 2009
Phase: N/A
Study type: Observational

The neutrophil-to-lymphocyte ratio (NLR) has been proven to be reliable inflammatory marker for atherosclerotic process and predictor for clinical outcomes in patients with various cardiovascular diseases. Recent study reported elevated NLR was associated with impaired myocardial perfusion in ST-segment elevation myocardial infarction (STEMI) patients. The investigators sought to determine whether NLR is associated with coronary microcirculation assessed by index of microcirculatory resistance (IMR) in STEMI patients who undergone primary percutaneous coronary intervention (PCI). A total of 123 patients with STEMI underwent successful primary PCI were consecutively enrolled. NLR at admission was calculated, and the patients were divided into three groups according to NLR tertiles. IMR was measured by intracoronary thermodilution-derived method immediately after index PCI.

NCT ID: NCT02822690 Completed - Cessation of Life Clinical Trials

Research Into the Quality of the Dying Phase

Start date: October 2016
Phase:
Study type: Observational

The aim of this study is to get insight in the quality of life at the end of life and quality of dying for patients died at the hospital in the department Groningen (the Netherlands). The primary endpoint is the quality of life at the end of life and the secondary endpoint is the quality of dying. Both according a numerical rating scale. An explorative analysis will be done for differences for the hospitals in Groningen, effect of using the Liverpool care Pathway for the dying, effect of using consultation by the palliative consultation team, effect of using the Hospice@UMCG intervention, correlation with the quality of life at the end of life and quality of dying according to nurses and doctors.

NCT ID: NCT02819973 Completed - Heart Failure Clinical Trials

Educational Videos to Address Racial Disparities in Implantable Cardioverter Defibrillator Therapy

VIVID
Start date: July 2016
Phase: N/A
Study type: Interventional

VIVID is a prospective, multicenter, randomized clinical trial in African American patients that will to evaluate: (1) the effect of an educational video on knowledge of sudden cardiac death (SCD) and implantable cardioverter defibrillators (ICDs); (2) the effect of an educational video on the decision for ICD implantation, decisional conflict, and receipt of an ICD within 90 days; and 3) the effect of racial concordance between study patients and video participants (health care providers/patients) on the decision for ICD implantation, decisional conflict and ICD receipt within 90 days.

NCT ID: NCT02800421 Completed - Clinical trials for Myocardial Infarction

Prognostic Impact of Organ Damage in STEMI Patients

Start date: January 2007
Phase: N/A
Study type: Observational [Patient Registry]

Besides contrast-induced acute kidney injury (CI-AKI), adscititious vital organ damage such as hypoxic liver injury (HLI) may affect the survival in patients with ST-elevation myocardial infarction (STEMI). Therefore, the investigator sought to evaluate the prognostic impact of CI-AKI and HLI in STEMI patients who underwent primary percutaneous coronary intervention (PCI).