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NCT ID: NCT00964067 Completed - Clinical trials for Coronary Artery Disease

Aerobic Interval Training in Cardiac Rehabilitation

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

The purpose of the study is to compare home-based aerobic interval training with supervised interval training performed in groups or on a treadmill at the hospital.

NCT ID: NCT00963534 Completed - Clinical trials for Mantle Cell Lymphoma

Lenalidomide, Bendamustine and Rituximab as First-line Therapy for Patients Over 65 Years With Mantle Cell Lymphoma.

LENA-BERIT
Start date: September 2009
Phase: Phase 1/Phase 2
Study type: Interventional

In phase I: Establishing maximally tolerated dose of lenalidomide in combination with bendamustine and rituximab. In phase II: Evaluation of progression free survival with treatment with lenalidomide, bendamustine and rituximab

NCT ID: NCT00963352 Recruiting - Colon Cancer Clinical Trials

Colon Cancer Prognosis After Radical Surgery

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

1. Radical surgery. It is supposed to improve prognosis of colon cancer. A surrogate measure of achievement of radical surgery is the number of lymph nodes removed with the specimen. 2. Markers. There may be variables that may make patient assessment more sound. The project is including investigation of such markers (genes, old age, comorbidity, and others). 3. Laparoscopic resections. This is being used more and more in cancer surgery but the feasibility of this approach remains to be proven compared with conventional open surgery. The project compares these according to 1) and 2). 4. Morbidity and mortality must be surveilled to keep at a minimum. Many patients have comorbidity and are old to make this factor extra important, including perioperative care. 5. Proper treatment of colon metastases may prolong life. Treatment of lung-metastases will be studied in particular.

NCT ID: NCT00962741 Completed - Clinical trials for Arthritis, Juvenile Idiopathic

Study Evaluating Etanercept in 3 Subtypes of Childhood Arthritis

CLIPPER
Start date: September 2009
Phase: Phase 3
Study type: Interventional

This study will evaluate the effect of etanercept on the clinical benefit, safety, and physical functioning (ability to function in daily life) in children and adolescent subjects with 3 subtypes of childhood arthritis.

NCT ID: NCT00962156 Completed - Septic Shock Clinical Trials

Scandinavian Starch for Severe Sepsis/Septic Shock Trial

6S
Start date: December 2009
Phase: Phase 3
Study type: Interventional

- By tradition hydroxyethyl starch (HES) is used to obtain fast circulatory stabilisation in critically ill. - High molecular weight HES may, however, cause acute kidney failure in patients with severe sepsis. - Now the low molecular weight HES 130/0.4 is the preferred colloid in Scandinavian intensive care units (ICU) and 1st choice fluid for patients with severe sepsis. - HES 130/0.4 is largely unstudied in ICU patients. - This investigator-initiated Scandinavian multicentre trial will be conducted to assess the effects of HES 130/0.4 on mortality and endstage kidney failure in patients with severe sepsis. - The trial will provide important data to all clinicians who resuscitate septic patients.

NCT ID: NCT00961844 Terminated - Clinical trials for Metastatic Malignant Melanoma

Trial for Vaccine Therapy With Dendritic Cells in Patients With Metastatic Malignant Melanoma

Start date: August 2009
Phase: Phase 1/Phase 2
Study type: Interventional

In this trial the investigators want to combine chemotherapy with immunotherapy by giving the patients Temozolomide, before vaccination. The investigators have also included hTERT and survivin mRNA in the vaccine. Finally, the investigators want to introduce ex vivo T cell expansion after lymphodepletion for the patients who show an immune response.

NCT ID: NCT00961740 Completed - Childhood Obesity Clinical Trials

Childhood Obesity- Characteristics and Treatment

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

The study is evaluating the effect of a 14-session cognitive behavioural treatment for childhood obesity. The treatment is family based and 49 families with children with obesity, aged 8-12, will be recruited. Outcome measures are: BMI, waist circumference, self-esteem, social- and psychological functioning, cholesterol, glucose and insulin values, activity level (actigraphs) and a measure of food intake.

NCT ID: NCT00960232 Completed - Hypovitaminosis D Clinical Trials

Vitamin D, Blood Pressure, Lipids, Infection and Depression

Start date: September 2009
Phase: Phase 3
Study type: Interventional

There are numerous indications for a relation between low serum levels of 25(OH)D and blood pressure, lipid levels, frequency of infections and tendency towards depression. Whether it is a causal relationship it is not known, and can best be studied with a vitamin D intervention. The investigators hypothesis is that supplementation with a high dose vitamin D (40.000 IU per week) will have a beneficial effect on these parameters.

NCT ID: NCT00960128 Completed - Clinical trials for Chronic Kidney Disease

Observational Prospective Study on Patients Treated With Norditropin®

Start date: April 1, 2006
Phase: N/A
Study type: Observational

This observational study is conducted globally. The aim of the study is to investigate the effectiveness and safety of real-life treatment with Norditropin®. The study population will consist of children and adults who are on treatment with Norditropin® in accordance with normal clinical practice.

NCT ID: NCT00959452 Completed - Hypochondriasis Clinical Trials

Follow up of Patients Treated With Cognitive Behavioural Therapy for Hypochondria From 1997 to 2007

Start date: January 1997
Phase: N/A
Study type: Interventional

Research has shown that cognitive behavioural therapy is effective in treating hypochondria. However, no studies have examined the long term effect. The investigators have followed 56 patients treated for hypochondria between 1997 and 2001 and the investigators are now doing a 10 year follow-up (Part I). In another part of the study (Part II) the investigators compare the effect of 16 sessions vs. 5 sessions, with a follow-up period of at least 2 years. The investigators hypothesis is that the initial 1 year improvement will be sustained and that 5 sessions will yield the same results as 16 sessions.