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NCT ID: NCT01099501 Recruiting - Multiple Trauma Clinical Trials

Oxepa in Multiple Trauma

OMT
Start date: April 2010
Phase: Phase 4
Study type: Interventional

This is a single-center, prospective, randomized, comparative, double-blind controlled clinical study mend to assess the effect of enteral feeding with Oxepa (a fish oil-based nutrition), compared to an isocaloric control, on oxygenation and clinical outcomes in mechanically ventilated trauma patients. The study population will be adults admitted to the ICU due to multiple-trauma or head trauma as a result of a gun shut, motor vehicle accidents, fall, workplace accident etc.

NCT ID: NCT01101152 Recruiting - Healthy Clinical Trials

Effectiveness of the Dual Serotonin Norepinephrine Reuptake Inhibitor Desvenlafaxine Succinate in Healthy Volunteers

DVS
Start date: April 2010
Phase: Phase 1
Study type: Interventional

DVS is the main metabolite of the antidepressant/anxiolytic medication Venlafaxine (Effexor). Like parent compound, DVS is an antidepressant inhibiting both serotonin (5-HT) and norepinephrine (NE) reuptake. However, no studies to date describe the in vivo potency of this drug on monoamines reuptake. Consequently, it appears essential to determine the potency of DVS in human subjects using a wide dose range in order to determine at which dose(s) it starts inhibiting 5-HT and NE reuptake. The investigators are interested in learning whether there is a gender difference in the dose of the study medication at which NE reuptake inhibition occurs.

NCT ID: NCT01101256 Recruiting - Clinical trials for Anticoagulant Prophylaxis/Therapy

Determination of Residual Anticoagulatory Effects of Fondaparinux

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

The purpose of this study is to determine residual anticoagulatory effects of a prophylactic or therapeutic fondaparinux treatment i.e. prior to surgery/intervention, after pause of therapy etc.

NCT ID: NCT01101295 Recruiting - Clinical trials for Purpura, Thrombocytopenic, Idiopathic

The ITP-RITUX Cohort: Rituximab in Immune ThrombocytoPenia.

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

The primary purpose of the study is to describe by a prospective observational study the serious adverse events occurring in patients treated off-label by rituximab for Immune Thrombocytopenia.

NCT ID: NCT01101503 Recruiting - Clinical trials for Endothelial Dysfunction

The Effect of Intensive Multifactorial Therapy on Endothelial Function in Newly Diagnosed Type 2 Diabetes

Start date: April 2010
Phase: Phase 2
Study type: Interventional

The endothelial dysfunction is the early event in atherosclerosis. The investigator previous study showed that impaired endothelial function exist in newly diagnosed type 2 diabetes. The investigators hypothesize that intensive multifactorial therapy including intensive blood control and intensive hypertension control as well as intensive blood lipids control of 1 year can improve vascular endothelial function. Moreover, the improvement of endothelial function maintains after 5 years or 10 years of intensive multifactorial therapy, called "Metabolic Memorial Effect of improvement of endothelial function".

NCT ID: NCT01102335 Recruiting - Clinical trials for Hepatocellular Carcinoma

Synergistic Treatment for Hepatocellular Carcinoma (HCC) Using Transcatheter Arterial Chemoembolization (TACE) With Anti-hepatitis B Virus (Anti-HBV) Therapy

TACEHBV
Start date: April 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to elucidate the influence of anti-hepatitis B virus therapy on safety and survival of HCC patient after transcatheter arterial chemoembolization.

NCT ID: NCT01102634 Recruiting - Healthy Subjects Clinical Trials

Effects of Acu-Transcutaneous Electrical Nerve Stimulation (Acu-TENS) on Post-exercise Blood Lactate and Excessive Post-exercise Oxygen Consumption (EPOC)

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

The study aims to investigate the effect of Acu-TENS on post-exercise blood lactate level and EPOC

NCT ID: NCT01102790 Recruiting - Thrombosis Clinical Trials

Generation of Heparin-induced Thrombocytopenia (HIT)-Antibodies Without Prior Heparin Exposure

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

The purpose of this study is to determine the HIT-antibody generation without prior heparin-exposure in patients undergoing orthopedic surgery.

NCT ID: NCT01103765 Recruiting - Implant Clinical Trials

Post-dilatation for Optimization of Drug-eluting Stents (DES) Deployment Assessed by Intravascular Ultrasound Multicenter Analysis

PODIUM
Start date: April 2010
Phase: Phase 4
Study type: Interventional

Comparison with use of Intravascular Ultrasound (IVUS) analysis of two methods of percutaneous coronary interventions (PCI) with drug eluting stent: After successful drug eluting stent implantation, patients were randomized into two groups: Group A had no further dilatation, and Group B had additional post-dilatation with a noncompliant balloon. The investigators performed IVUS analysis in groups A and B just before randomization and after post-dilatation in group B.

NCT ID: NCT01104623 Recruiting - Clinical trials for Attention-Deficit/Hyperactivity Disorder

ADHD - Voice Analysis, Vocal Acoustic Biomarkers in Attention Deficit Hyperactivity Disorder

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

The purpose of this study is to detect specific vocal acoustic patterns in the voice of attention deficit hyperactivity disorder (ADHD) patients.