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NCT ID: NCT01133184 Not yet recruiting - Liver Fibrosis Clinical Trials

Improved Prevention of Perinatal Hepatitis B Transmission

Start date: September 2010
Phase: Phase 4
Study type: Interventional

Impaired activity of Natural Killer (NK) cells has been proposed as a mechanism contributing to viral persistence in Hepatitis C Virus (HCV) infection. NK cells display anti-fibrotic activities by killing activated hepatic stellate cells (HSCs) that have lost the self-recognition marker; Major Histocompatibility (MHC) class I. Determining the down-expressed genes on NK cells necessary for their anti-fibrotic activity was never studied previously. This will allow us to study their role fully in phagocytosis process as well as their interaction of HSCs and therefore manipulating these genes using molecular techniques. Exploring the cellular functions of these genes will highlight their involvement in the progression of liver fibrosis and could be used as a therapeutic tool for preventing the disease.

NCT ID: NCT01133080 Recruiting - Schizophrenia Clinical Trials

Minocycline as an Adjunctive Therapy for Schizophrenia: a Randomized Controlled Study

Start date: June 2010
Phase: Phase 4
Study type: Interventional

Double - Blind, Randomized, single centered study. The purpose of this study is to assess the feasibility of minocycline vs. placebo, added to atypical antipsychotic medications, for positive symptoms in adults suffering from schizophrenia.

NCT ID: NCT01132742 Completed - Malnutrition Clinical Trials

Malnutrition and Outcome in Hospitalized Children in Europe

Start date: February 2010
Phase: N/A
Study type: Observational

Malnutrition in children has even more severe consequences on disease course and long-term health than malnutrition in adults. According to prior studies, malnutrition affects about 15-30 % of hospitalized children in Europe (ESPGHAN 2005, Pawellek et al 2008, Joosten and Hulst 2008). However, available criteria for defining malnutrition in paediatric patients are inconsistent, not based on firm evidence, and not generally agreed upon. Current guidelines do not address assessment of and screening for childhood malnutrition. Therefore, a large number of affected children are not adequately diagnosed. One aim of this study is to assess the prevalence of malnutrition and patients at risk for malnutrition among at least 2700 hospitalized children mainly across Europe. In addition criteria to link anthropometric measurements and the prediction of outcome, i.e. length of hospital stay, shall be established. A further goal then is to establish agreed, evidence-based criteria for malnutrition in children with the purpose of leading to an agreed, evidence-based screening tool for paediatric malnutrition in developed countries. This tool shall include a set of simple questions, based on previously suggested tools. Thereby this study will provide a strong basis for implementing evidence-based nutritional interventions in paediatric patients by harmonisation of diagnostic criteria for childhood malnutrition in developed countries.

NCT ID: NCT01132690 Completed - Gaucher Disease Clinical Trials

A Safety and Efficacy Study of Two Dose Levels of Taliglucerase Alfa in Pediatric Subjects With Gaucher Disease

Start date: August 2010
Phase: Phase 4
Study type: Interventional

This is a multi-center, double-blind trial to assess the safety and efficacy of taliglucerase alfa in untreated subjects (2 to <18 years old) with Gaucher disease randomly assigned to treatment with one of two doses, 30 or 60 units/kg. Subjects will receive an intravenous (IV) infusion of taliglucerase alfa every two weeks. The total duration of treatment will be 12 months. At the end of the 12-month treatment period eligible subjects will be offered enrollment in an open-label extension study if taliglucerase alfa is not commercially available.

NCT ID: NCT01132612 Completed - Clinical trials for Plaque-type Psoriasis

AIN457 Regimen Finding Extension Study in Participants With Moderate to Severe Psoriasis

Start date: May 11, 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study was to provide long term clinical data for the compound for the treatment of the indication of moderate to severe chronic plaque-type psoriasis.

NCT ID: NCT01132300 Completed - Low Back Pain Clinical Trials

Efficacy Study Image Guided, Auto-Targeted Neurostimulation for the Treatment of Non-Specific Low Back Pain

Start date: July 2009
Phase: N/A
Study type: Interventional

The purpose of this study is: - Initial evaluation of the clinical effectiveness of Image Guided Transcutaneous Electrical Stimulation (TENS) device for treatment of non-specific low back pain. - To assess the tolerability and acceptability of the device by the caregiver ("User Friendly"). - To evaluate patients' tolerance by monitoring side effects and tolerability during treatment.

NCT ID: NCT01131676 Completed - Clinical trials for Diabetes Mellitus, Type 2

BI 10773 (Empagliflozin) Cardiovascular Outcome Event Trial in Type 2 Diabetes Mellitus Patients (EMPA-REG OUTCOME).

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

The aim of the present study is to investigate the safety of BI 10773 treatment in patients with Type 2 Diabetes Mellitus and high cardiovascular risk.

NCT ID: NCT01131663 Recruiting - Infant Clinical Trials

Design and Development of an Infant's Oriented Face Mask

Start date: April 2010
Phase: N/A
Study type: Observational

Face masks are used for many respiratory care applications such as anaesthesia, resuscitation, and aerosol therapy. None of the currently available face mask for infants and young children are specifically designed and developed for infants. The aim of this study is to design, develop and test the first infant's oriented face mask. To achieve this ultimate goal we will first define appropriate sizes of infants' faces that would be used as templates for the design and development of optimally fitted model masks. In the next stage we will use these masks and incorporate the infants' own soother (pacifier) into a new SootherMask (SM). In the last part of the study we will compare acceptance levels between Soothermask (SM) and a conventional commodity masks without a pacifier.

NCT ID: NCT01130038 Completed - Clinical trials for Development Coordination Disorder

Characteristic of Play: Comparison Between Children With Development Coordination Disorder ( DCD) and Children With Typical Development

Start date: August 2010
Phase: N/A
Study type: Observational

There will be found differences in the issue of characteristic of play between Children with Development Coordination Disorder and Children with Typical Development.

NCT ID: NCT01129934 Not yet recruiting - Low Back Pain Clinical Trials

Morphine Versus Morphine-promethazine Combination for Acute Low Back Pain Relief in the Adult Emergency Department

Start date: May 2010
Phase: Phase 4
Study type: Interventional

Acute low back pain is a common cause for emergency department visits. Controversy remains regarding the optimal medication for acute low back pain relief. The investigators hypothesized that administration of pharmacological anxiolysis in addition to analgesia will improve pain relief and patient management in the emergency department.