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NCT ID: NCT01679717 Recruiting - Clinical trials for Thumb Osteoarthritis

Postoperative Therapy After Interposition Arthroplasty in CMC1

Start date: June 2012
Phase: N/A
Study type: Interventional

In this randomized controlled trial the investigators want to investigate whether early versus late mobilisation after surgery in the first carpometacarpal joint (CMC1) leads to a faster recovery of hand function. The investigators also want to explore patients' satisfaction with the two different treatment regimes. The participants in the control group will receive the standard treatment at Diakonhjemmet hospital: immobilisation of the thumb in a splint for six weeks. The participants in the intervention group will use a soft splint for six weeks, but will be instructed to remove the splint daily to perform exercises for the thumb. A total of 70 patients will be included in the study.

NCT ID: NCT01679496 Completed - Dietary Prevention Clinical Trials

Fat Quality on Blood Lipids and Immune Response

NoMa
Start date: June 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate blood LDL-cholesterol and level of inflammatory markers after intake of food items with different fatty acid composition.

NCT ID: NCT01677143 Completed - Pain, Postoperative Clinical Trials

Pre-emptive Local Anaesthesia in Gynecological Laparoscopy

Start date: February 2013
Phase: Phase 4
Study type: Interventional

Pre-emptive local anaesthetics are widely used in laparoscopic surgery, but there is no really consistent evidence that it is useful. Studies in the literature have shown contradicting results. At our hospital we are currently using pre-emptive local anaesthetics in the trocar areas, but as the literature does not give a clear and clinically relevant answer, we need to find out more. This study aims to see if pre-emptive local anaesthetics are useful in the setting of our day-case, laparoscopic surgery.

NCT ID: NCT01676883 Completed - Obesity, Morbid Clinical Trials

Plantar Callosities and the Validity of Body Composition Assessment by Bio-impedance in Severely Obese Persons

Start date: October 2012
Phase: N/A
Study type: Interventional

Studies have confirmed the association between plantar callosities and severely obese individuals. Bioelectrical impedance analysis (BIA) is an increasingly popular tool for estimating body composition because it is easy to use, noninvasive, relatively inexpensive, and can be performed across a wide range of subjects. Our hypotheses for this study are: (1)plantar callosities influence the body composition measurements obtained by bioelectrical impedance analysis BIA, and (2) BIA underestimates the percentage of body fat compared with air-displacement plethysmography (BodPod).

NCT ID: NCT01676870 Completed - Metabolic Syndrome Clinical Trials

Exercise in Prevention of Metabolic Syndrome

EX-MET
Start date: January 2012
Phase: N/A
Study type: Interventional

The primary objective of the study is to compare in a real-world setting the efficacy of traditional training (today's guideline, vigorously or moderate exercise) and amount of aerobic interval training (1-AIT) in reduction of risk factors constituting metabolic syndrome. The secondary objective is to compare the efficacy of traditional moderate training (today's guideline) and amount of aerobic interval training (1-AIT vs. 4-AIT) in improving aerobic capacity, cardiovascular function, skeletal muscle contractile function, skeletal muscle energy metabolism, left ventricle systolic and diastolic function at rest and right ventricular function. The investigators hypothesized that aerobic interval training would reverse features of the metabolic syndrome more than traditional training.

NCT ID: NCT01675713 Completed - Morbid Obesity Clinical Trials

Lifestyleintervention for the Treatment of Severe Obesity

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

The overall purpose of this project is to study the acute, short- (≤ 1 year) and long- (> 1 year) term effects on body composition and psychological health after a 10 to 14-weeks comprehensive lifestyle modification program for the treatment of severe obesity. The aims of the PhD project are to investigate whether an intensive lifestyle intervention leads to acute and short term (< 1 year) changes in: 1. The BMI/Weight 2. Body composition (waist circumference, fat mass, fat free mass, skeletal muscle mass and visceral fat area) 3. Psychosocial factors such as eating behavior, anxiety and depression symptoms and health-related quality of life

NCT ID: NCT01675180 Recruiting - Pregnancy Clinical Trials

Self Reported Oral Health, Awareness and Attitude Towards Dental Care Among Pregnant Women

Start date: February 2013
Phase: N/A
Study type: Interventional

Purpose/Objective of the study: The main objective of the study is to investigate oral health awareness and attitudes towards oral health among Norwegian pregnant women and assess the impact of information about oral hygiene on the risk of dental caries during pregnancy. The hypothesis of the study are: 1. The state of oral health during pregnancy depends on pregnant woman's preventive oral hygiene behaviour and practice. 2. Pregnant women with high level of oral health awareness and positive attitude towards oral health are more likely to visit their dentists regularly and have better oral hygiene compared to those with less awareness. 3. Proper information and guidance on oral hygiene care provided during pregnancy can help to improve oral bacteriological milieu and reduce the dental caries risk among pregnant women.

NCT ID: NCT01674556 Completed - Clinical trials for Pancreatic Adenocarcinoma

Ultrasound-assisted Treatment of Inoperable Pancreatic Cancer

Start date: February 2012
Phase: Phase 1
Study type: Interventional

The investigators primary aim is to increase chemotherapeutic drug uptake in inoperable tumours The specific sub-objectives of the studies are: - To quantify tumour sizes and relate it to the patient survival over time, dependent of treatment method. - To evaluate and compare the toxic effects and safety of gemcitabine in combination with US contrast agent under sonication with gemcitabine alone. - Develop and validate new ultrasound perfusion algorithms based on burst- replenishment for diagnosis and monitoring of therapy. - To quantify gemcitabine and its main metabolites in plasma and in circulating mononuclear cells before, during and after pancreatic sonication, and to quantify the concentration of intracellular endogenous nucleotides in circulating mononuclear cells at the same time points. - To assess plasma and tissue concentrations of gemcitabine, its main metabolites and endogenous nucleotides in those patients where surgical resection can be performed on standard clinical indications.

NCT ID: NCT01674114 Completed - Pregnancy Clinical Trials

Postoperative Morphine Consumption After Caesarean Section- TAP Block vs Intracutaneous Infiltration

Start date: September 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether a regional-block (TAP block) in Caesarean section will give a measurable benefit in form of reducing Morphine consumption as compared to local infiltration of the wound with local anesthetic.

NCT ID: NCT01673867 Completed - Clinical trials for Non-Squamous Cell Non-small Cell Lung Cancer

Study of BMS-936558 (Nivolumab) Compared to Docetaxel in Previously Treated Metastatic Non-squamous NSCLC

CheckMate057
Start date: November 2, 2012
Phase: Phase 3
Study type: Interventional

The purpose of the study is to compare the overall survival of BMS-936558 (Nivolumab) as compared with Docetaxel in subjects with non-squamous cell non-small cell lung cancer (NSCLC) after failure of prior platinum-based chemotherapy