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NCT ID: NCT01433120 Completed - Obesity Clinical Trials

Targeting the Gut Microbiome to Investigate the Pathways of Progression From Obesity to Metabolic Diseases in an At-risk Population.

Start date: September 2011
Phase: N/A
Study type: Interventional

Studies of the human gut microbiome have suggested that treatment or prevention aimed at the obese microbiome could influence the development of obesity-associated metabolic disturbances. The objective of this project is to explore if a dietary intervention in 60 obese women with the probiotic Lactobacillus paracasei ssp paracasei F19 or flax seed fibres targeting the gut microbiome, can reduce insulin resistance, low-grade inflammation or dyslipidaemia, and to explore the interaction between the human genome and the gut microbiome. The study is based on the following hypotheses: - Treatment with the probiotic Lactobacillus paracasei ssp paracasei F19 and flax seed fibres will lower the metabolic risk profile in the intervention groups compared with placebo. - The effect on the metabolic risk markers can be correlated with changes in the gut microbiota (measured in faeces). After completion of the dietary intervention, the participants are offered a 10-week weight reduction program. Those who participate in the weight-loss program are invited to an optional follow-up visit in connection with the last visit at the clinical dietician, for the purpose of exploring the effect of weight loss on the gut microbiota and obesity-associated metabolic disturbances.

NCT ID: NCT01432691 Completed - Optimized Treatment Clinical Trials

Hemi Artificial Hipjoint Versus Total Artificial Hipjoint

THA
Start date: June 2010
Phase: Phase 4
Study type: Interventional

This is a Randomized Controlled Trial study comparing hemialloplastik versus total joint replacement.

NCT ID: NCT01432197 Completed - Clinical trials for HRQOL (Health Related Quality of Life)

Occupational Therapy for Cancer Patients: a Randomised, Controlled Study

Start date: March 2010
Phase: Phase 0
Study type: Interventional

The aim of this study is to investigate the effect of occupational therapy, in shape of activities of daily living, for cancer patients.

NCT ID: NCT01431274 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Tiotropium+Olodaterol Fixed Dose Combination (FDC) Versus Tiotropium and Olodaterol in Chronic Obstructive Pulmonary Disease (COPD)

Start date: September 2011
Phase: Phase 3
Study type: Interventional

The overall objective of this study is to assess the efficacy and safety of 52 weeks once daily treatment with orally inhaled tiotropium + olodaterol FDC (delivered by the RESPIMAT Inhaler) compared with the individual components ( tiotropium, olodaterol) (delivered by the RESPIMAT Inhaler) in patients with Chronic Obstructive Pulmonary Disease (COPD).

NCT ID: NCT01431261 Completed - Neck Pain Clinical Trials

Neck Exercises, Training and Pain Management as a Treatment for Whiplash Patients With Chronic Neck Pain

WADNECXT
Start date: January 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to test whether a physiotherapy intervention containing pain management, general training and specific neck exercises can improve function for patients with chronic neck pain.

NCT ID: NCT01431092 Completed - Schizophrenia Clinical Trials

Melatonin Versus Placebo for Benzodiazepine Discontinuation in Patients With Schizophrenia

SMART
Start date: October 2011
Phase: Phase 4
Study type: Interventional

In this trial, researchers aim to investigate if prolonged-release melatonin can facilitate the withdrawal of chronic benzodiazepine administration in patients with schizophrenia. Furthermore, researchers will investigate the association of benzodiazepine dose reduction with the following clinically important variables: sleep, psychophysiology, cognition, social function, and quality of life.

NCT ID: NCT01430676 Completed - Incisional Hernia Clinical Trials

Risk Factors for Morbidity After Incisional Hernia Repairs

Start date: January 2007
Phase:
Study type: Observational

The Danish Ventral Hernia Database (DVHD) registers 37 different perioperative parameters. The aim of present study is to use large-scale data from DVHD to uncover risk factors for readmission, reoperation (any indication), death and reoperation for recurrence after incisional hernia repair.

NCT ID: NCT01430520 Completed - Postoperative Pain Clinical Trials

Analgesic Effect of Escitalopram in Total Knee Arthroplasty (TKA)

Start date: September 2011
Phase: Phase 4
Study type: Interventional

Pain is a major problem after TKA, especially in patients with high pain catastrophizing. Newer MR-scan studies indicate that Escitalopram may have an immediate cognitive and emotional effect. The investigators therefore investigate the effect of Escitalopram as a perioperative analgesic.

NCT ID: NCT01430481 Completed - Osteoarthritis Clinical Trials

Rosehip Powder for Knee Osteoarthritis

Start date: August 2011
Phase: Phase 2
Study type: Interventional

The aim of this study is to compare three combinations of preparations in a comparative trial program on rosehip powder for knee OA. The trial is a comparative, 12-week, randomized, double-blind, active-controlled trial, designed to determine the comparative efficacy and safety of these preparations in patients with pain from knee OA.

NCT ID: NCT01430143 Completed - Clinical trials for Diabetes Mellitus, Type 2

Physical Activity for a Long and Healthy Life

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

The aim of the study is to 1) delineate the molecular mechanisms behind the large variation in insulin sensitivity among apparently healthy subjects and to 2) establish the dose-response relationship between physical training and a) metabolic health, b) appetite and c) cultural health.