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NCT ID: NCT01195441 Completed - Preeclampsia Clinical Trials

Prediction and Prevention of Preeclampsia by First Trimester Ultrasound

Screen-tox
Start date: September 2010
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether the Fetal Medicine Foundation algorithm for individual risk calculation for preeclampsia (PE) and pregnancy induced hypertension (PIH) is suitable to identify women in high risk of developing these diseases in a Norwegian population.

NCT ID: NCT01194570 Completed - Clinical trials for Multiple Sclerosis, Primary Progressive

A Study of Ocrelizumab in Participants With Primary Progressive Multiple Sclerosis

Start date: March 2, 2011
Phase: Phase 3
Study type: Interventional

This randomized, parallel group, double-blind, placebo controlled study will evaluate the efficacy and safety of ocrelizumab in participants with primary progressive multiple sclerosis. Eligible participants will be randomized 2 : 1 to receive either ocrelizumab or placebo.

NCT ID: NCT01193543 Completed - Overweight Clinical Trials

Effect of Calanus Oli on Intra-abdominal Fat, Glucose Tolerance and Lipids in Man

Start date: December 2010
Phase: Phase 2/Phase 3
Study type: Interventional

Preliminary studies in rats and mice indicate that calanus oil reduce accumulation of intra-abdominal fat. Pilot studies in humans have shown no adverse effects. In the present study 120 subjects, males and females, 20-65 years old, BMI 25-30 kg/m2 will be included and given calanus oli 1 g twice daily versus placebo for 1 year. The hypothesis is that calanus oil will reduce intra-abdominal fat, improve glucose tolerance and lipid profile.

NCT ID: NCT01190280 Completed - Gallstones Clinical Trials

Indications for Gallbladder Surgery in Gallstone Disease

Start date: October 1991
Phase: Phase 3
Study type: Observational

The aim of the study is to identify patients with gallstone disease that should be operated and those that may potentially be observed. This selection was based on symptoms and clinical presentation. The consequences that may arise for the patient if observation is chosen compared with outcome after cholecystectomy has been markers of outcome.

NCT ID: NCT01185821 Completed - Clinical trials for Relapsing Remitting Multiple Sclerosis

Long-term Safety, Tolerability and Efficacy of BAF312 Given Orally in Patients With Relapsing-remitting Multiple Sclerosis

Start date: August 30, 2010
Phase: Phase 2
Study type: Interventional

This study consisted of a two year dose blinded phase during which patients received one of five doses of siponimod (10, 2, 1.25, 0.5 or 0.25mg) following which patients were switched to open label treatment with siponimod 2mg for approximately a further 3 years. It will provide data on long term safety, tolerability and efficacy of siponimod in the RRMS patient population

NCT ID: NCT01184937 Completed - Renal Recipients Clinical Trials

Effect of Patient Education on Kidney Recipients Knowledge, Coping and Quality of Life

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

For patients with end-stage kidney disease, transplantation is the treatment of choice, offering improved quality of life by restored metabolism and freedom from dialysis. However, demands regarding the acquirement of knowledge in life post transplantation are high. In order to reduce rejection episodes, graft loss and the negative consequences of life-long immunosuppressive medication, it is essential for kidney recipients to possess knowledge about important aspects regarding immunosuppressive medication, graft surveillance and the benefit of specific lifestyle behavior. Consequently, patient education is required for this patient group. This randomized controlled trial is investigating the effect of a structured patient education program on kidney recipients' knowledge, coping and quality of life

NCT ID: NCT01184768 Completed - Type 2 Diabetes Clinical Trials

HBA1c and Diagnosis of Type 2 Diabetes

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

Following the 6th Tromso study subjects with HbA1c > 5.7 plus a subsample of subjects with lower hba1c values will be invited to an oral glucose tolerance test to see the predictive value of HBA1c in the diagnosis of type 2 diabetes.

NCT ID: NCT01183351 Completed - Dementia Clinical Trials

Multidisciplinary Intervention for Challenging Behaviour (Agitation) in Patients With Dementia

TID
Start date: May 2011
Phase: N/A
Study type: Interventional

The increasing prevalence of dementia is a major challenge to the health authorities in most countries. Nearly all the persons suffering from dementia experience behavioural and psychological symptoms (BPSD). The prevalence of BPSD is particularly high in nursing homes. BPSD are often treated with psychotropic drugs even though the evidence for effect is minimal and the risk of serious adverse events is considerable. All the major treatment recommendations advise that non-pharmacological measures should be applied first when treating BPSD even though the evidence for such treatment is limited. The investigators will conduct a pilot study of a non-pharmacological treatment for BPSD. The method has been developed in Norway and has already been implemented in a number of nursing homes in the county of Nordland.

NCT ID: NCT01182935 Completed - Type 2 Diabetes Clinical Trials

Elevated Triglyceride Levels and Later Type 2 Diabetes

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

Subjects with elevated serum triglycerides in the 4th Tromso study in 1994/1995 were re-examined with an oral glucose tolerance test to see predictive value of triglycerides regarding development of type 2 diabetes

NCT ID: NCT01182870 Completed - Influenza Clinical Trials

Vitamin D and the Influenza Epidemic

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

Subjects included in ongoing vitamin d intervention trials were asked by questionnaire if they were ill with influenza during the winter season 2009/2010 to see if vitamin d supplementation prevented flu like disease.