Clinical Trials Logo

Filter by:
NCT ID: NCT00196482 Recruiting - Premature Birth Clinical Trials

Human Milk Fortifiers and Acid-Base Status

Start date: June 2004
Phase: N/A
Study type: Interventional

Double-blind randomized controlled trial to investigate the impact of two human milk fortifiers on acid-base status and longitudinal growth and weight gain in preterm infants. Two different compositions are tested, main difference is in electrolyte composiiton.

NCT ID: NCT00196469 Recruiting - Hemorrhage Clinical Trials

Impact of Heparin on the Need for Mechanical Ventilation in Neonates

Start date: December 2003
Phase: Phase 4
Study type: Interventional

This study is designed to test an incidental finding of a previous trial in which post hoc analysis showed that the rate of intensive care newborns requiring mechanical ventilation was lower in the group receiving heparin with the continuous infusion as compared to the placebo group.

NCT ID: NCT00196248 Recruiting - Clinical trials for Ventricular Fibrillation

Out-of Hospital Resuscitation Study

Start date: n/a
Phase: Phase 4
Study type: Observational

Sudden cardiac arrest is one of the most common causes of death in industrial countries. The main objective of this study is to built up a register of all out-of hospital resuscitation in a defined area. According to this register, it is possible to evaluate for example predictors of survival to improve training and organisation of prehospital resuscitations.

NCT ID: NCT00196209 Recruiting - Atrial Fibrillation Clinical Trials

Cardioversion vs. Catheter Ablation for Persistent Atrial Fibrillation

Start date: August 2005
Phase: Phase 4
Study type: Interventional

The aim of this randomized study is to evaluate the efficacy of two different approaches for conversion of persistent atrial fibrillation, the non-invasive one (external electrical cardioversion) and the invasive one (catheter ablation).

NCT ID: NCT00196157 Recruiting - Atrial Fibrillation Clinical Trials

Line Versus Spot Ablation in Persistent Atrial Fibrillation

Start date: August 2004
Phase: Phase 4
Study type: Interventional

In this randomized study dealing with the ablative treatment of persistent atrial fibrillation, two ablation strategies are compared: a more anatomically guided linear ablation scheme versus an electrophysiological guided focal ablation strategy aiming at the electrical isolating of the pulmonary veins and ablating areas of fragmented intracardiac electrograms thought to maintain atrial fibrillation.

NCT ID: NCT00188149 Recruiting - Hodgkin Disease Clinical Trials

Optimization of the Primary Therapy for Patients With Hodgkin's Disease and Evaluation of PET

Start date: May 2000
Phase: Phase 4
Study type: Interventional

Prognosis of patients with Hodgkin´s lymphoma (HL) has been improved significantly over the last decade. Therefore, the impact of treatment associated long-term toxicities and late effects such as second cancers increased. The purpose of this prospective multicenter trial is to show the feasibility of the treatment with ABVD alone in patients with limited stage (HL1) and intermediate stage (HL2) disease and of an intensified etoposide-free chemotherapy regimen for patients with advanced disease (HL3) including 18F-FDG-PET evaluation.

NCT ID: NCT00180206 Recruiting - Arthritis Clinical Trials

Birmingham Hip Resurfacing (BHR) Study: Implantation of a Hip Resurfacing Endoprosthesis

Start date: January 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is the investigation of the functional and radiological results and subjective patient outcome after the implantation of a hip resurfacing endoprosthesis (Birmingham hip resurfacing).

NCT ID: NCT00180128 Recruiting - Clinical trials for Leukemia, Promyelocytic, Acute

AIDA2000 - Risk-Adapted Therapy for Patients With Acute Promyelocytic Leukemia

Start date: January 2000
Phase: Phase 4
Study type: Interventional

In AIDA 2000 therapy of acute promyelocytic leukemia (APL) is given in a risk-adapted manner. Risk factors are age and white-blood-cell (WBC)-count at diagnosis. Induction therapy is done with ATRA and idarubicin followed by postremission therapy with daunorubicin and mitoxantrone in age adapted dosages. Patients with an high WBC were additionally treated with cytarabine. Finally a two year period of maintenance therapy with 6-mercaptopurine, methotrexate and ATRA is performed.

NCT ID: NCT00176410 Recruiting - Clinical trials for Aortic Valve Stenosis

Statin Therapy in Asymptomatic Aortic Stenosis

Start date: January 2003
Phase: Phase 2
Study type: Interventional

There is evidence that the degenerative changes leading to aortic stenosis are caused by a chronic inflammatory process. Furthermore the development of aortic stenosis is partially dependent on typical cardiovascular risk factors. An inflammatory process as well as those risk factors are amenable for medical therapy. As such the use of statins (HMG CoA reductase inhibitors) would be an appealing concept to reduce both those risks for development of aortic stenosis. Aim of this study is to evaluate the usefulness of statin therapy on the progression of aortic stenosis.

NCT ID: NCT00176397 Recruiting - Clinical trials for Coronary Artery Disease

Percutaneous Coronary Intervention (PCI) With Drug-Eluting Stents (DES) Versus Coronary Artery Bypass Graft (CABG) for Patients With Significant Left Main Stenosis

Start date: August 2003
Phase: Phase 2
Study type: Interventional

Recent technical advances in percutaneous coronary interventions have made it possible to approach patients with coronary lesions formerly considered to be classical candidates for bypass surgery, e.g. patients with left main coronary stenosis. However, it is still unclear whether the good long-term results achieved with the surgical therapy can be reproduced by an interventional strategy using drug-eluting stents (DES). The aim of the current trial is, therefore, to compare the clinical and angiographic results of PCI and CABG in patients with left main coronary stenosis.