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NCT ID: NCT00379522 Completed - Shock Clinical Trials

Vasopressin in Traumatic Hemorrhagic Shock Study

Start date: July 2010
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of the present trial is therefore to assess effects of arginine vasopressin vs. saline placebo on hospital admission rate (primary end point), as well as hemodynamic variables, fluid resuscitation requirements and hospital discharge rate (secondary study end points) in presumed traumatic hemorrhagic shock patients with a systolic arterial blood pressure <90 mm Hg after 10 min of standard shock treatment. Accordingly, the study reflects an add-on design to standard traumatic shock therapy. The hypothesis is that both arginine vasopressin and saline placebo have comparable effects on hemodynamic variables, fluid resuscitation requirements, and hospital admission and discharge rate. The alternative hypothesis is that arginine vasopressin has more beneficial effects on hemodynamic variables, fluid resuscitation requirements, and hospital admission and discharge rate than saline placebo.

NCT ID: NCT00379470 Completed - Clinical trials for Recurrent Glioblastoma Multiforme

Effect of NovoTTF-100A in Recurrent Glioblastoma Multiforme (GBM)

Start date: September 2006
Phase: Phase 3
Study type: Interventional

The study is a randomized, controlled trial, designed to test the efficacy and safety of a new medical device, the NovoTTF-100A. The device is an experimental, portable, battery operated device for chronic treatment of patients with recurrent or progressive glioblastoma multiforme (GBM) using alternating electric fields (termed TTFields).

NCT ID: NCT00378014 Completed - Clinical trials for Liver Transplantation

Preservation of Renal Function in Liver Transplant Recipients With Certican Therapy

Start date: August 2006
Phase: Phase 3
Study type: Interventional

The study is designed to show that everolimus initiation together with reduction and thereafter discontinuation of calcineurin inhibitor (CNI) will improve significantly renal function in de novo liver transplant recipients as compared to continuation of CNI-based treatment.

NCT ID: NCT00377728 Completed - Clinical trials for Seasonal Allergic Rhinitis

Trial With Rhinitic Patients Taking GSK256066 Versus Placebo In A Pollen Challenge Chamber

Start date: March 2006
Phase: Phase 2
Study type: Interventional

This study is in patients with seasonal allergic rhinitis(SAR)and will compare the effect versus placebo of repeat doses of intranasal GSK256066 using the Vienna Challenge Chamber. GSK256066 is a potent and highly selective phosphodiesterase-4 (PDE4) inhibitor, currently in development by GSK for the treatment of allergic rhinitis, asthma and COPD. Subjects will be selected on the basis that they display a defined moderate response to the pre-determined dose used. Opportunity to assess the efficacy of compounds versus placebo at maximal and trough plasma concentrations. This study aims to explore the actions of repeat doses of intranasal GSK256066 in patients with Seasonal Allergic Rhinitis in the Vienna Challenge Chamber compared to placebo. 12-lead ECG, vital signs and adverse event enquiries will be made throughout the study. Nasal examination, symptom scores (TNSS), nasal lavage, nasal scrape and allergen challenge assessments will also be performed at various time points throughout the study.

NCT ID: NCT00376116 Completed - Clinical trials for Heart Failure, Congestive

Home Monitoring in Cardiac Resynchronisation Therapy

HomeCARE
Start date: March 2005
Phase: N/A
Study type: Observational

In spite of success in the management of heart failure, repetitive rehospitalisation and high mortality rate remain a serious problem. Recent studies, especially the COMPANION trial, have demonstrated that cardiac resynchronisation therapy (CRT) reduces mortality and rehospitalisation in heart failure patients. There is also evidence that telemonitoring of heart failure patients potentially reduces both mortality and morbidity. Recently, a Home Monitoring (HM) function has been integrated into BIOTRONIK CRT-defibrillators and CRT-pacemakers with a view of harnessing the powerful combination of CRT with close remote monitoring of heart failure patients. It is possible now to transmit predefined parameters on a daily basis from the implanted devices to a web-based platform accessible by patients' physicians. Our study evaluates clinical usefulness of Biotronik HM function in CRT-defibrillators and CRT-pacemakers.

NCT ID: NCT00375323 Completed - Hemophilia A Clinical Trials

Recombinant Factor VIIa (NovoSeven) on Restoring Coagulation Activation

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of the study is to compare the effects of recombinant factor VIIa (NovoSeven) on restoring coagulation activation between patients with hemophilia A and antibodies to factor VIII and normal subjects (controls) by use of an in vivo method.

NCT ID: NCT00375076 Completed - Cancer Clinical Trials

Comparison of Two Different Dosages of Low-molecular Weight Heparin in Cancer Patients

Start date: June 2006
Phase: Phase 3
Study type: Interventional

In a prospective, randomized, double-blind trial, the effects of two different dosages of LMWH (5000 anti-Xa U od sc and 10 000 anti-Xa U od sc daily) on markers of hemostatic system and thrombin generation will be investigated in non-surgical cancer patients will be investigated.

NCT ID: NCT00373646 Completed - MALT Lymphoma Clinical Trials

Thalidomide in Mucosa Associated Lymphoid Tissue (MALT) Lymphoma Patients

Start date: June 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate Thalidomide for treatment of disseminated MALT Lymphoma or at relapse following helicobacter pylori (HP) - eradication or chemotherapy or radiation.

NCT ID: NCT00373425 Completed - Clinical trials for Non-small Cell Lung Cancer

A Study of Erlotinib (Tarceva) After Surgery With or Without Adjuvant Chemotherapy in Non-Small Cell Lung Carcinoma (NSCLC) Patients Who Have Epidermal Growth Factor Receptor (EGFR) Positive Tumors

RADIANT
Start date: September 2006
Phase: Phase 3
Study type: Interventional

This is a study to evaluate the effectiveness of erlotinib compared with a placebo sugar pill following complete surgical removal of the tumor with or without chemotherapy after surgery in Stage IB-IIIA NSCLC patients.

NCT ID: NCT00372385 Completed - Chronic Hepatitis C Clinical Trials

Phase 2 Study of VX-950, Pegasys® With and Without Copegus® in Hepatitis C

Start date: August 2006
Phase: Phase 2
Study type: Interventional

Compare the effectiveness of telaprevir (VX-950) in combination with Pegylated Interferon Alfa 2a (Peg-IFN-alfa-2a) with and without Ribavirin (RBV) in reducing plasma hepatitis C virus (HCV) ribonucleic acid (RNA) levels