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NCT ID: NCT01082770 Enrolling by invitation - Clinical trials for Central Line Infection

Randomised Controlled Trial of Needle Free Access Devices in Preventing Hemodialysis Blood Stream Infection

TEGO
Start date: March 2010
Phase: Phase 4
Study type: Interventional

This study will be a randomised controlled trial examining whether a new type of needle free access device(TEGO) is associated with less episodes of infection of dialysis lines, when compared to the current gold standard. The investigators hypothesise that there will be less handling of the dialysis line by nursing staff and thus this will lead to lower rates of infection. The investigators will also assess whether these access devices lead to alterations in catheter blood flow rates when compared to the current gold standard.

NCT ID: NCT01078844 Enrolling by invitation - Autism Clinical Trials

Memantine in Adult Autism Spectrum Disorder

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

The purpose of this study is to see if memantine is helpful in managing problematic symptoms in adults with autism, Asperger's disorder, or Pervasive Developmental Disorder NOS.

NCT ID: NCT01063192 Enrolling by invitation - Clinical trials for Locally Advanced Pancreatic Cancer

A Study of Locally Advanced Pancreatic Cancer

Start date: November 2009
Phase: Phase 2
Study type: Interventional

The primary end point is to evaluate the time to progression after gemcitabine alone versus Gemcitabine-based combination induction chemotherapy followed by concurrent chemoradiotherapy in locally advanced pancreatic cancer. The secondary end points are to evaluate the disease control rate, overall survival time, toxicity profile and compliance after induction chemotherapy and concurrent chemoradiotherapy as well as the disease control rate after inductional chemotherapy alone in locally advanced pancreatic cancer. Translational research including pharmacogenomic study and biomarker study will also be done concomitantly.

NCT ID: NCT01053299 Enrolling by invitation - Clinical trials for Developmental Dysplasia of the Hip (DDH)

Universal Ultrasound-screening for Developmental Dysplasia of the Hip in Newborn

Start date: March 2010
Phase: N/A
Study type: Interventional

All newborn from the period 12.1988 to 31.12.2006 During the two last decades, hip ultrasound has gained acceptance as an accurate screening test for developmental dysplasia of the hip (DDH) and for monitoring the development and treatment of the condition. Debate continues over whether DDH that is detected by ultrasonography is necessarily clinically relevant. The diagnostic accuracy of ultrasound imaging for DDH in the screening population has not been investigated adequately. Studies that investigate the natural course of the disorder, the optimal treatment for DDH, and the best strategy for ultrasound screening are needed. Ultrasound screening at birth for DDH in all newborn infants is standard practice in some European countries but not in the United Kingdom, the United States, or Scandinavia. Evidence is insufficient to support or reject general ultrasound screening of newborns for DDH. (N.F.Woolacott etc 2006, systematic review BMJ) At Vestre Viken HF, Kongsberg, Norway, the investigators implemented universal ultrasound screening in 1998. We will present the long term outcome, including radiographs of the hips after 5-12 years.

NCT ID: NCT00969644 Enrolling by invitation - Clinical trials for Interaction Between the GH/IGF-I System and the Immune-system

The Relationship Between the Growth Hormone (GH)- Insulin Like Growth Factor I (IGF-I) System and the Inflammatory System in Healthy Normal Persons

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

Observations in patients with growth hormone (GH)-disturbances have suggested that GH/IGF-I might have anti-inflammatory effects. To elucidate this hypothesis the investigators have planned a study to investigate if 3 weeks administration of GH and subsequently the GH antagonist Pegvisomant (or vice versa) influence serum levels of different inflammatory markers in healthy volunteers.

NCT ID: NCT00964093 Enrolling by invitation - Clinical trials for Central Line Bloodstream Infections

The Effectiveness of Silver Alginate (Algidex) Patch in the Prevention of Central Line Infections in Very Low Birth Weight Infants

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

The purpose of this study is to determine whether silver alginate (Algidex) patch is effective in the prevention of central line infections in very low birth weight infants.

NCT ID: NCT00933660 Enrolling by invitation - Clinical trials for Improvement of BLS/AED Training Methods

Retention and Retrieval for Three Different Training Methods

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

The hypotheses that will be studied are: H0: Providers trained by a web based application for skill competency in basic life support (BLS) and automated external defibrillation (AED) are as competent as those who were trained by certified instructors using the European Resuscitation Council (ERC) curriculum H00-1: Providers who trained themselves with the used of web based training are more competent when they had a personal manikin for home exercise compared to providers who trained themselves with only a web based training H0-2: Providers who did not receive any training will score lower than those who did. Research questions for this study are: 1. What are the results in skill competency for non trained people? 2. What are the results in skill competency for trained people immediately after training? 3. What is the retention of skills for trained and non trained people after six months?

NCT ID: NCT00932906 Enrolling by invitation - Clinical trials for Improvement of BLS/AED Training Programmes

Comparison of Different Automated External Defibrillation (AED) Training Methods

Start date: July 2008
Phase: N/A
Study type: Interventional

This study is a prospective, randomized trial that compares the effectiveness and retention of four different training methods for the use of an AED: A. Traditional instructor based learning; B. The use of a personal manikin with a DVD training to practice the necessary AED skills; C. The use of a personal manikin with a DVD training to practice the necessary AED skills and additional scenario training; D. Watching a 2.5 minutes DVD which shows the use of an AED. It is hypnotised that there are no differences between these training methods, in which case method D is most efficient to reach large number of people to learn BLS/AED skills. There are two interesting target groups to reach: 1. Younger people, as they might give the highest interest after training, as they normally live longer. 2. Older people as they are member of the most important group in risk and have therefore a higher change of being a witness of cardiac arrest. As there might be differences in the results between different training methods than can be related to age, each training group is distinguished to three different groups: 1. 21 years of younger; 2. between 21 and 50 years; 3. older than 50 years. It is hypnotised that there are no differences between younger and older students within each of the four training methods.

NCT ID: NCT00932711 Enrolling by invitation - Clinical trials for Pulmonary Disease, Chronic Obstructive

Effect of Educational Intervention in Patients With Low-Risk Chronic Obstructive Pulmonary Disease

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

The purpose of this study is to determine if educational intervention is effective in reducing exacerbations of chronic obstructive pulmonary disease in patients with low-risk disease.

NCT ID: NCT00925184 Enrolling by invitation - Clinical trials for Understand Students' View Toward Current Medical Education.

Students' View: Survey of Medical Education in Taiwan

Start date: July 2008
Phase: N/A
Study type: Observational

The aim of this research project is to establish a students' perspective to most medical schools in Taiwan. We expect that these surveys will provide helpful information to candidates for selection of medical school before admission, and will also be a useful reference guide to improve quality of medical education to our governmental policy makers.