Clinical Trials Logo

Filter by:
NCT ID: NCT02613429 Completed - Clinical trials for Upper Airway Obstruction

Identification of Airway Structures Necessary for Airway Access Via the Skin

Start date: November 2015
Phase: N/A
Study type: Interventional

Literature shows that anaesthetists have a low success-rate when trying to access the airway percutaneously in case of failed ventilation and intubation. The study will investigate anaesthetists ability to locate the trachea and the thyroid cartilage and the cricoid cartilage in patients, using different methods including application of ultrasonography.

NCT ID: NCT02612467 Completed - Low Back Pain Clinical Trials

Low Back Pain - What's Next? Stratified Care Compared to Current Practice

Start date: November 2015
Phase: N/A
Study type: Interventional

Background Studies in the United Kingdom find the stratified care model of the STarT Back Tool (SBT) to be superior to usual care in primary care low back pain (LBP) patients. However, considerations on differences in health care and social systems across countries are required before taking steps towards any recommendations of implementing stratified care into other health care services. Objective To investigate the effectiveness of the stratified care model of the SBT, when embedded into the regional disease management programs on LBP in primary care as compared to current best practice care.

NCT ID: NCT02612103 Completed - Crohn Disease Clinical Trials

Biomarkers in Inflammatory Bowel Diseases

Start date: November 2015
Phase:
Study type: Observational [Patient Registry]

Ulcerative colitis (UC) and Crohn's disease (CD) are chronic relapsing inflammatory bowel diseases (IBD). At the time of diagnosis it is not possible to predict the course of the disease, which can range from a few flares in a lifetime to uncontrollable disease leading to hospitalization, surgery and stoma. There is a continuous need to improve diagnostic and prognostic tools. In chronic inflammation diseases there is an excessive turnover of the extracellular tissue. Tissue is broken down to small fragments and released into the circulation. Changes in the amount of these fragments in the blood may provide information on the damage and quality of the affected tissue and may therefore act as objective measure of disease burden and severity - a so called biomarker. The potential of such biomarkers is evaluated in a combined cross-sectional and longitudinal survey including 300 patients with UC, CD, irritable bowel disease and healthy controls. The patients are followed for up to 1 year. Changes in biomarker are correlated to standard markers of inflammation during active disease and remission. Perspective The use of new biomarkers may offer a tool to evaluate early changes in the gut of patients with IBD, may be a supplement to the diagnosis, serve as markers for effect of treatment and prognosis, and in time be a good alternative to fecal samples or endoscopy.

NCT ID: NCT02611830 Completed - Colitis, Ulcerative Clinical Trials

Efficacy and Safety of Vedolizumab Subcutaneously (SC) as Maintenance Therapy in Ulcerative Colitis

Start date: December 18, 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the effect of vedolizumab subcutaneous (vedolizumab SC) maintenance treatment on clinical remission at Week 52 in participants with moderately to severely active ulcerative colitis (UC) who achieved clinical response following administration of vedolizumab intravenous (vedolizumab IV) induction therapy.

NCT ID: NCT02611817 Completed - Crohn's Disease Clinical Trials

Efficacy and Safety of Vedolizumab Subcutaneous (SC) as Maintenance Therapy in Crohn's Disease (CD)

Start date: January 4, 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the effect of vedolizumab subcutaneous (vedolizumab SC) as maintenance treatment in participants with moderately to severely active CD who achieved clinical response following administration of vedolizumab intravenous (vedolizumab IV) induction therapy.

NCT ID: NCT02610907 Completed - Ileostomy Clinical Trials

A Pilot Evaluation of Adhesives and How They Are Impacted by Out-put

Start date: November 2015
Phase: N/A
Study type: Interventional

The study investigates the impact real output (subjects own) and simulated output have on the adhesion of adhesives.

NCT ID: NCT02610803 Completed - Ischemic Stroke Clinical Trials

Paroxysmal Atrial Fibrillation in Patients With Acute Ischemic Stroke

Start date: September 2014
Phase: N/A
Study type: Observational

The purpose of this study is to estimate the clinical relevance of monitoring patients with acute ischemic stroke with 48 hours' inpatient cardiac telemetry in relation to evaluate the presence of brief runs of premature atrial complexes and new diagnosed atrial fibrillation. Furthermore to evaluate the prognostic significance of brief runs of premature atrial complexes in relation to develop atrial fibrillation, recurrent stroke/transient ischemic attack and death.

NCT ID: NCT02609334 Completed - Asthma Clinical Trials

RSPR-007 Mannitol Challenge Trial

Start date: March 2015
Phase: Phase 2
Study type: Interventional

This is a double-blind, randomised, placebo-controlled, cross-over, Phase 2 trial evaluating two doses (a low and a high) of CRD007 for the treatment of asthmatic trial subjects with a positive asthma test (mannitol challenge) prior to enrolment.

NCT ID: NCT02608372 Completed - High Blood Glucose Clinical Trials

Brown Seaweeds Effect on Glucose Tolerance and Appetite Response

Start date: May 2015
Phase: N/A
Study type: Interventional

The project is a randomized, 3-way, blinded crossover trial in which 20 healthy, fasted participants consume meals with 30 g of a linear corn starch and 5 g of one of the seaweeds, Laminara digitata or Undaria pinnatifida or a pea protein control. The primary aim is to investigate whether the brown seaweeds affect the postprandial glucose Area Under the Curve (AUC). Stomach emptying, insulin, C-peptide, appetite-regulating hormones (oxyntomodulin, glucagon, GLP-1 and PYY), and specific metabolites from the seaweeds in the urine and plasma as well as subjective satiety are also analyzed.

NCT ID: NCT02607358 Completed - Clinical trials for Acute Ischemic Stroke

Non-responders to Antiplatelet Treatment in Acute Ischaemic Stroke)

NATIS
Start date: January 2015
Phase: N/A
Study type: Observational

Determination of frequency of Clopidigrel- and Acetacylicacid-non-responders (HOTPR) in acute ischemic stroke patients.