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NCT ID: NCT00235339 Completed - Clinical trials for Myocardial Infarction

Effect of Standard Care Rehabilitation Versus Interval Treadmill Training After Myocardial Infarction

Start date: October 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effect of the standard rehabilitation offered by three hospital rehabilitation units in Norway, one in Trondheim, one in Ålesund and one in Levanger, compared to an interval treadmill training program. The subjects participating in the study are patients with myocardial infarction. The maximal oxygen consumption of the subjects will be tested before and after the training period.

NCT ID: NCT00233350 Completed - Brain Neoplasms Clinical Trials

Clinical Evaluation of Navigated 3D Ultrasound Multicentre Study

Start date: January 2007
Phase: N/A
Study type: Observational

3D ultrasound is a new modality used in image guided neurosurgery. a multicentre study is started for the evaluation of this tool as a means for achieving total resection of brain tumors at greater safety.

NCT ID: NCT00232726 Completed - Neoplasm Metastasis Clinical Trials

Clinical Study of Previously Untreated Patients With Malignant Melanoma

Start date: September 2005
Phase: Phase 2
Study type: Interventional

Previously untreated patients with malignant melanoma receive a new chemotherapy drug currently under development. CP-4055 is given intravenously on days 1-5 every four weeks until complete response or disease progression.

NCT ID: NCT00232492 Completed - Tooth, Impacted Clinical Trials

Ketamine on Acute Pain in Females and Males

Start date: January 2005
Phase: Phase 4
Study type: Interventional

The purpose of the study is to determine whether equal subanesthetic doses of racemic ketamine is equally effective on females and males after surgical removal of third molars

NCT ID: NCT00230919 Completed - Obesity Clinical Trials

Weight Loss and Changes in Cardiovascular Risk Markers With a Low Glycemic Diet Compared With a Standard Diet

Start date: April 2004
Phase: N/A
Study type: Interventional

Overweight and obesity is increasing in most countries, including Norway, and the optimal diet for reducing weight is under discussion. The present study in overweight and moderate obese individuals compares a low glycemic load diet with a standard low-fat diet (as recommended from the National Nutrition Council) in an open, randomized trial over 12 months, with changes in weight loss and changes in cardiovascular risk markers as endpoints.

NCT ID: NCT00229151 Terminated - Bipolar Disorder Clinical Trials

Sleep Deprivation and Advancement of Sleep Period as Treatment for Bipolar Depression.

Start date: October 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if sleep deprivation and sleep phase advancement is effective treatment of bipolar patients in a depressive phase.

NCT ID: NCT00227084 Completed - Mammaplasty Clinical Trials

Effect of Arista Powder on Bleeding in Reductive Mammary Surgery

Start date: September 2005
Phase: Phase 2
Study type: Interventional

To evaluate whether Arista AH which contains microporous polysaccharides used as a powder applied to the wound area during mammary surgery reduces the amount of bleeding and the duration of surgery. Both mammae are operated on in the same procedure, and one side without Arista serves as control side

NCT ID: NCT00226889 Terminated - Clinical trials for Systemic Sclerosis (Scleroderma)

Treatment of Early Systemic Sclerosis by Bosentan

TRANOS
Start date: January 2005
Phase: Phase 1/Phase 2
Study type: Interventional

Systemic sclerosis (ssc) is characterised by extensive tissue fibrosis. Using drugs that are capable of inhibiting fibroblast activity may be beneficial if administrered early in the disease course. Thirty adult patients with early SSc will be treated with the endothelin-1 antagonist bosentan for 6 months.Disease progression will be assessed.

NCT ID: NCT00226733 Terminated - Clinical trials for Coronary Artery Bypass

Training Intensity After Coronary Bypass Grafting

Start date: March 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate the effect of high and moderate intensity exercise training after coronary bypass surgery. The subjects are randomised to training at either 60-70% or 85-95% of their maximal capacity daily for four weeks. Primary outcome measure is change in maximal aerobic capacity, measured as change in maximal oxygen consumption, after the training period. Secondary outcome measures are change in quality of life, heart rate variability, ultrasound measures of the heart and blood variables, including endothelian markers.

NCT ID: NCT00226499 Completed - Varicella Clinical Trials

Evaluate Vaccine Against Chickenpox and a Combined Vaccine Against 4 Viral Childhood Diseases: Measles, Mumps, Rubella and Chickenpox

Start date: September 1, 2005
Phase: Phase 3
Study type: Interventional

An observer-blind study to evaluate GlaxoSmithKline Biologicals' live attenuated varicella vaccine and GlaxoSmithKline Biologicals' combined measles-mumps-rubella-varicella vaccine in the prevention of varicella disease in children. The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep 2007.