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NCT ID: NCT01838603 Completed - Chronic Pain Clinical Trials

Patient Experience of Interventional Pain Management. Qualitative Study

Start date: April 2013
Phase: N/A
Study type: Observational

There are quite a few qualitative studies done to find out patients experience of chronic pain. There are no studies on what the patients feel and what thoughts and feelings arise in the patients that are exposed to interventional pain management. This study aims to illuminate how it is to live through an interventional pain management program.

NCT ID: NCT01838473 Completed - Smoking Cessation Clinical Trials

In-vivo Extraction of Lead, Cadmium and Tobacco Specific Nitrosamines From Swedish 'Snus' in Regular Snus Users

SMWS03
Start date: May 2004
Phase: Phase 1
Study type: Interventional

In an open label, randomized, two-way cross-over study, 32 male healthy regular snus users will be given repeated doses of four different types of portion snus: "General", "Catch", "Catch Mini" and "Catch Dry Mini". Each portion of used snus will be collected and frozen (-20 oC) pending analysis of lead (Pb), cadmium (Cd), nicotine and tobacco specific nitrosamines (TSNAs). Unused snus is collected and deep frozen for analysis and calculation of extracted dose. Calculations of extracted amount of lead, cadmium, nicotine and tobacco specific nitrosamines (TSNAs) respectively, will be done for each type of snus.

NCT ID: NCT01838460 Completed - Smoking Cessation Clinical Trials

Sublingual Nicotine Tablets Compared With Swedish Snus

Start date: May 2012
Phase: Phase 1/Phase 2
Study type: Interventional

To compare each subject's AUCinf, after administration of one single dose of 6 mg of Nicorette sublingual nicotine tablets ( three 2mg tablets) to that of one single 1 g dose of SS containing 16 mg nicotine.

NCT ID: NCT01837940 Completed - Constipation Clinical Trials

Efficacy of a Dietary Supplementation With Lactobacillus Reuteri for Digestive Health in an Elderly Population

Start date: April 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the effect of a daily supplement consisting of the probiotic bacteria, Lactobacillus reuteri, on the digestive health among persons 65 years and older.

NCT ID: NCT01837550 Completed - Hearing Impaired Clinical Trials

Educational Program for Hearing Aid Users With Internet Support

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

The purpose of this study is to examine the short-term effects of complementing an educational program for hearing aid users with Internet support.

NCT ID: NCT01836796 Completed - Type 2 Diabetes Clinical Trials

Metabolic Effects of Lactobacillus Reuteri DSM 17938 in Type 2 Diabetes

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

Recent data suggest that the trillions of bacteria in gastrointestinal tracts (gut microbiota) can function as an environmental factor that modulates the amount of body fat. Obese individuals have an altered gut microbiota and germ-free mice are resistant to developing diet-induced obesity and have lower fasting insulin and glucose concentrations and shows an improved glucose tolerance. Administration of the probiotic bacterium Lactobacillus Gasseri SBT2055 in fermented milk for 12 weeks reduced adiposity and body weight in obese adults possibly by reducing lipid absorption and inflammatory status. However, there are no controlled studies to the investigators knowledge that address whether probiotic supplementation affects glucose metabolism. The investigators hypothesis is that supplementation of Lactobacillus reuteri DSM 17938 may improve metabolic control in type 2 diabetes patients. In addition, the investigators will explore possible mechanisms behind the antihyperglycemic action of Lactobacillus Reuteri.

NCT ID: NCT01836666 Completed - Chronic Pain Clinical Trials

Effects on Health Related Quality of Life Among Patients With Chronic Pain by Interventional Pain Management

Start date: January 2008
Phase:
Study type: Observational [Patient Registry]

How are the health related quality of life among patients with chronic pain effected by interventional pain managment? Hypothesis: Health related quality of life can be improved by interventional pain management both among patients with localizable pain focuses and among patients among whom no pain focuses can be found. Method: Health related quality of life using EQ-5D and EQ-VAS is registered at first visit, at the time of treatment for pain focuses an during the following 12 months.

NCT ID: NCT01836523 Completed - Diabetes Clinical Trials

The Efficacy and Safety of Liraglutide as Adjunct Therapy to Insulin in the Treatment of Type 1 Diabetes

ADJUNCT ONEā„¢
Start date: November 2013
Phase: Phase 3
Study type: Interventional

This trial is conducted globally. The aim of the trial is to confirm the efficacy and safety of liraglutide as adjunct therapy to insulin in the treatment of type 1 diabetes. The total trial duration per subject is approximately 58 weeks.

NCT ID: NCT01835704 Completed - Chronic Pain Clinical Trials

Health-economic Evaulation of Interventional Pain Mangement

Start date: January 2008
Phase:
Study type: Observational

To establish the cost per QALY (Quality Adjusted life Years) gained all patients that are referred to a specialized interventional pain clinic are assessed by Euroqol EQ-5D to measure the health-related quality of life at the first visit and then during the following year. Quality of life is calculated from EQ-5D by using hte TTO-validated UK-value set. With this and calculations of the cost we will be able to calculate the cost per QALY-gained which makes it possible to compare interventional pain managment to other treatments for pain patients.

NCT ID: NCT01831271 Completed - Cervical Pain Clinical Trials

Neck-specific Training or Prescribed Physical Activity for Patients With Cervical Radiculopathy

Start date: August 2010
Phase: N/A
Study type: Interventional

The overall objective is to evaluate if treatment with a neck-specific exercise program and cognitive behavioural approach improves the outcome compared with prescribed, self-mediated and progressive physical activity in patients with cervical radiculopathy. There is a lack of evidence of the best treatment for the patient category. Many patients are sick-listed for long periods of time with different kind of treatment approaches or without any treatment at all. The present study could fill the identified knowledge gap by strengthening of the currently weak scientific evidence for treatment of the patient category. The long-term effects of the study could be to reduce the time for sick leave and improve the rate of patients returning to work and/ or former activity by optimising treatments. Further on, to decrease the number of patients who finally have surgery for their neck problems and thus reducing the mental, physical and social costs.