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NCT ID: NCT00848263 Completed - Clinical trials for Distal Radius Fractures

Unstable Fractures of the Distal Radius: Trial of Volar Plate Versus Dorsal Nail Plate Fixation

RADIUS
Start date: February 2009
Phase: N/A
Study type: Interventional

Fractures of the distal radius are one of the most common orthopaedic injuries and are associated with a high complication rate. There is a lack of clinical trials comparing the different treatment modalities of fractures of the distal radius. The purpose of this randomized trial is to assess differences in functional outcome, radiological results, and complication rate in patients 55 years and older with an unstable displaced fracture of the distal radius without articular involvement treated with a dorsal nail plate or a volar plate.

NCT ID: NCT00844727 Terminated - Duodenal Polyposis Clinical Trials

Coxib-inhibition of Duodenal Polyp Growth in FAP

Start date: September 2003
Phase: Phase 2/Phase 3
Study type: Interventional

Preliminary data indicate a protective effect on the development of duodenal polyps by coxib treatment. The hypothesis of the present study is that normal therapy doses of rofecoxib for 1 year would stop or reverse the development of premalignant adenomatous lesions in the duodenal mucosa of FAP patients.

NCT ID: NCT00843193 Completed - Asthma Clinical Trials

Efficacy and Safety Study of GSK679586 in Patients With Severe Asthma

Start date: December 9, 2008
Phase: Phase 2
Study type: Interventional

Treatment, Randomised, Double Blind, Parallel Assignment, Safety/efficacy Study

NCT ID: NCT00842777 Completed - Childhood Obesity Clinical Trials

Childhood Obesity: a Study of Group Treatment Targeting Parents Behaviour

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

Long term effects of treatment of childhood obesity are not well documented but there is growing evidence that parental involvement and behavioral changes are strong predictors of children weight loss. However, which form and content of parental involvement are most effective is not studied. In the present randomized controlled study we compare the effect of parent manualized group treatment ("experimental group") to the effect of parent self-help groups on changes in children Body Mass Index, food intake, physical activity, quality of life and self esteem. We pose the following hypotheses: 1. Parents participating in the experimental group will have children who achieve a larger reduction in BMI than children with their parents in the control group. 2. This treatment effect will be mediated by changes in one of several elements of parents' cognition: outcome expectancies, perceived control, perceived value of outcome, self-efficacy, perceived reduction in barriers, and subjective norms. 3. Reduction in BMI will correlate with increased quality of life, reduced number and severity of mental health problems, and increased self-concept.

NCT ID: NCT00842387 Completed - Heartburn Clinical Trials

Evaluation Study of a Management Strategy for Gastroesophageal Reflux Disease (GERD)

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

The aim of this project is to compare the GERD clinical outcomes in patients where a structured pathway using the GerdQ questionnaire is implemented compared with the clinical outcomes of those treated without this implementation. This is a European project with 5 participating countries (Austria, Italy, Norway, Spain and Sweden). Due to different characteristics regarding the actual management of this disease in the 5 countries, each country had the flexibility to introduce design differences and changes in the study protocol.

NCT ID: NCT00840697 Recruiting - Low Back Pain Clinical Trials

Effect of Interventions in Return to Work for Patients With Neck and Low Back Pain

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

Low back pain is a usual condition in the western countries and several treatments available for patients with "non-specific low back pain". According to the European guidelines both Brief intervention and exercise/cognitive intervention are effective treatments with regard to pain and function (www.backpaineurope.org), but none have documented effect on return to work. The challenges for health personnel is not cure of the patients back pain, but to build up rehabilitation programs which focus on disability and work incapacity, in patients which are at risk of loosing their work. Dr. P. Loisel, Montreal, Canada", has since 1995 treated patients with back pain according to the "The PREVICAP model - (PREVention of work handICAP)", where the main purpose with work-related program is to prevent prolonged disability and to help patients back to work. Loisel demonstrated that the PREVICAP models accelerated the "return to work" factor by a factor 2.4 (p=0.01). The PREVICAP model had also been evaluated in Amsterdam, by Dr. Anema with the same results. At the Back Clinic, Ullevål University Hospital we are presently involved in a randomized controlled trial after the PREVICAP model, where patients are randomized to Brief intervention including a work-related intervention or usual care. All included patients in both groups, will have a clinical examination by specialist in Physical Medicine and Rehabilitation and advice from a physiotherapist. The current study replaces Brief intervention with an exercise - and a work-related program, so patients with non-specific LBP will be randomized to an exercise and work-related program or usual care. The main purpose of this study - to investigate if rehabilitation programs specifically focusing on the return to work process will reduce sickness absence and disability pension in patients with neck and low back pain. - to assess the work-, individual- and health factors and their interrelationship predicting sickness absence and work disability. - to compare results from the rehabilitation program with results from rehabilitation program in Toronto - to which extent are the patients met by actions from employers and employment services, and does is influence sickness absence and disability. - do these actions represent favourable cost benefit for the work places and the society

NCT ID: NCT00840229 Completed - Adhesive Capsulitis Clinical Trials

Rotator Interval and Intra-articular Corticosteroid Injection for Frozen Shoulder

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

The purpose of this study is to compare ultrasound guided capsular corticosteroid injection into the rotator interval/anterior capsule and the GH joint with ultrasound guided corticosteroid injection into the GH joint only. Both methods will be compared with placebo injections. Primary outcome measure: pain reduction at week 6 Secondary outcome measures: improvement of function (SPADI, Life quality, ROM). 0-hypothesis: no difference between the methods. The investigators want to find out if the clinical effect of the combined capsular and intra-articular injections are better than placebo and better that intra-articular injections

NCT ID: NCT00839826 Completed - Thromboembolism Clinical Trials

ODiXahip - a Phase IIa Dose Escalating Proof of Principle Trial

ODiXaHip
Start date: December 2002
Phase: Phase 2
Study type: Interventional

Patients undergoing surgery, especially hip and knee surgery, are at high risk for VTE (up to 60 % without prophylaxis). The administration of drugs for thromboprophylaxis, such as heparins, significantly lowers that risk, but heparins have to be applied below the skin (subcutaneously). Additionally, there is a chance of developing a heparin-induced thrombocytopenia (decrease in platelets). Therefore, there is still a need for new agents which are safer and more efficient and which are easier to apply.The purpose of this study is to compare the safety and efficacy of BAY 59-7939 with the safety and efficacy of the licensed drug Enoxaparin. Enoxaparin, a so-called low molecular heparin, is approved and widely used in the area of thromboprophylaxis and will be given once daily subcutaneously.Another important purpose of the study is to find the optimal dose of BAY 59-7939 for thromboprophylaxis after hip replacement surgery. Therefore, there are several dose steps planned.

NCT ID: NCT00839579 Completed - Obesity Clinical Trials

Cardiovascular Treatment

Start date: January 2009
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 aim of this study is to investigate the amount of high-intensity exercise needed to improve aerobic capacity and endothelial function.

NCT ID: NCT00837070 Completed - Clinical trials for Zygapophyseal Synovial Joint Cyst

Percutaneous Rupture of Zygapophyseal Joint Cysts

Start date: January 2009
Phase: Phase 2
Study type: Interventional

Lumbar zygapophyseal joint cysts can cause lower extremity radiculopathy. These cysts can be cured by a minimally invasive technique: percutaneous cyst distention and rupture