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NCT ID: NCT01044940 Completed - Clinical trials for Colloid Osmotic Pressure

Measurements of Colloid Osmotic Pressure in Interstitial Fluid and Plasma in Healthy and Sick Children

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

The purpose of this study is to measure colloid osmotic pressure in interstitial fluid and plasma in healthy children under two years, in asphyxiated babies and in children undergoing heart surgery.

NCT ID: NCT01044641 Completed - Clinical trials for Colloid Osmotic Pressure

Measurement of Colloid Osmotic Pressure in Plasma and Interstitial Fluid in Children

Start date: December 2009
Phase: N/A
Study type: Observational

The purpose of this study is to identify normal values of colloid osmotic pressure in interstitial fluid and plasma in healthy children between 2 and 10 years.

NCT ID: NCT01042132 Completed - Clinical trials for Systemic Inflammatory Response Syndrome

Intramedullary Femoral Reaming, Human Study

Start date: May 2003
Phase: N/A
Study type: Interventional

To what extent the cardiopulmonary and inflammatory response is affected by initial femoral intramedullary nailing in the already traumatized and inflammatory activated patient was analyzed in the present study with the attention to survey the additional burden of this operative treatment. The patients are monitored with a pulmonary catheter, and blood samples for coagulation, fibrinolysis, complement and cytokine response are withdrawn pre-, per- and postoperatively. The study is partly randomized 1)where delayed intramedullary nailing is compared with primary nailing of the femur, and 2) a new reaming technique (RIA) is compared with a standard reaming technique (TR).

NCT ID: NCT01042067 Suspended - Atrial Fibrillation Clinical Trials

Safer Warfarin Treatment

CYKOWAR
Start date: January 2010
Phase: N/A
Study type: Observational

The study is a national multicenter prospective observational study, including 200 patients. The main purpose of this study is to explore in more detail the influence of genetic variability (CYP enzymes and vitamin K dependent proteins) and dietary vitamin K status on warfarin dosing, clinical effect and adverse events with emphasis on the initial phase of treatment. The hypothesis is that genetic variability concerning CYP enzymes and vitamin K dependent proteins predict dosing and adverse events during warfarin treatment. The main aim is to individualize warfarin therapy and establish a treatment algorithm based on genotype and dietary vitamin K status to make the anticoagulation therapy with warfarin more secure.

NCT ID: NCT01042002 Completed - Morbid Obesity Clinical Trials

Effect of Exercise Before Gastric Bypass

Start date: August 2006
Phase: N/A
Study type: Interventional

Exercise training is proved to protect against premature cardiovascular mortality. Additionally there is evidence that relatively high exercise intensity may be an important factor for improving aerobic capacity and endothelial function in patients with post-infarction heart failure, metabolic syndrome, coronary artery disease, as well as in overweight and obese individuals. The aims of this study is to investigate if High-intensity exercise before a gastric bypass operation will decrease hospitalization days and complications after the gastric bypass.

NCT ID: NCT01040728 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

A Randomized, Double-Blind, 4-way Crossover Study to Evaluate the Efficacy of of 24 Hour Spirometry Profiles of Inhaled BI 1744 CL and Inhaled Tiotropium Bromide in Patients With Chronic Obstructive Pulmonary Disease

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

The study is intended to characterize the lung function profile of BI1744 in Chronic Obstructive Pulmonary Disease (COPD) patients where patients will perform pulmonary function tests at regular intervals for 24 hours at the end of a 6 week treatment period. Each patient will receive all four treatments.

NCT ID: NCT01040429 Completed - Clinical trials for Chronic Fatigue Syndrome

The Norwegian Study of Chronic Fatigue Syndrome in Adolescents: Pathophysiology and Intervention Trial

NorCAPITAL
Start date: February 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study IS to - explore the underlying pathophysiology of chronic fatigue syndrome (CFS) in adolescents, particularly focusing on genetics, infections/immunology, endocrinology, autonomic control and cognitions - to assess the effect of clonidine (a drug that attenuates sympathetic nervous activity) in adolescent CFS.

NCT ID: NCT01039376 Terminated - Clinical trials for Leukaemia, Lymphocytic, Chronic

Ofatumumab Maintenance Treatment vs No Further Treatment in Relapsed CLL Responding to Induction Therapy

PROLONG
Start date: May 6, 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study was to determine if maintenance therapy with ofatumumab would prolong remission in patients with CLL who have responded to second or third line treatment. This study would also evaluate the safety of ofatumumab maintenance compared to observation (the current standard of care). This study was co-developed with the HOVON and NORDIC CLL group and would be conducted as a collaborative effort with GSK.

NCT ID: NCT01038960 Completed - Clinical trials for Ventricular Tachycardia

Exercise Training in ICD Recipients; Effect on Therapy Delivered, Depression and Anxiety

ETHIC
Start date: April 2008
Phase: Phase 3
Study type: Interventional

Interventional study in patients with ICD. Controlled, open intervention with exercise training. Assessment of changes in physiological and psychological parameters.

NCT ID: NCT01038141 Terminated - Clinical trials for Symptomatic Haemorrhoidal Disease

Recto Anal Repair or Milligan Morgans Operation of Grade 3 and 4 Symptomatic Haemorrhoidal Disease

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

The purpose of this study is to compare a new mini invasive surgical procedure (Recto Anal Repair) to the traditional Milligan-Morgan procedure in patients suffering from severe piles.