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NCT ID: NCT02002299 Recruiting - Colorectal Cancer Clinical Trials

Does Surface Tell us About the Invasive Front in Colorectal Cancer

CRC1
Start date: August 2013
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to investigate the invasive front in growth mode (expanding or infiltrative) and dedifferentiation (tumor budding) and comparing these with the tumor surface (polypose or flat) + / - ulceration in surgical specimens at colorectal cancer.

NCT ID: NCT02001805 Recruiting - Type 2 Diabetes Clinical Trials

Marathon Runners Compared to Sedentary Matched Control Subjects

Start date: December 2010
Phase: N/A
Study type: Observational

The investigators wish to compare very active runners in healthy untrained control subjects on a number of parameters. The project aims to understand the underlying mechanisms by which physical inactivity causes diseases. This the investigators will study the full spectrum of physical activity, from the most inert of the most active people. The investigators have already collected muscle biopsies and established stem cells from people with Type 2 diabetes, obese healthy and normal weight healthy. In this study, the investigators will establish a cohort of highly physically active marathon runners. In a case-control design, the investigators compare muscle stem cell function across the entire spectrum of physical activity / inactivity.

NCT ID: NCT02001766 Recruiting - Type 2 Diabetes Clinical Trials

ATP Release and Sympathetic Nerve Activity in Patients With Type II Diabetes

Start date: February 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Type II diabetes (T2D) is characterized by endothelial dysfunction, resulting in a poor tissue perfusion and function as well as an increased risk of cardiovascular events. ATP, which is released from the red blood cells, contributes to the regulation of the blood flow and studies have shown that red blood cells taken from T2D patients have an impaired ability to release ATP. However, it is not known whether the changes in the ATP system is an underlying cause of the poor tissue perfusion observed in T2D. The purpose of project 1 is to test the hypothesis that the deterioration in blood flow in T2D is caused by a reduced release ATP from red blood cells, and to test if pharmacological manipulation of cAMP will normalize ATP release, plasma ATP levels and thereby blood flow. Furthermore, epidemiological studies show a clear link between regular exercise and a reduced risk of serious cardiovascular disease. The extent to which a physically active lifestyle may improve endothelial function in T2D is unknown. Regular physical activity improves vascularization and induces an anti-inflammatory environment. Both the angiogenic and anti-inflammatory effects of physical activity is in part mediated by substances released from the active muscle. These muscle-derived substances are classified as myokines and have paracrine, autocrine and endocrine effects and may thereby affect distant tissues. The purpose of the project 2 is to investigate whether high intensity interval training may reverse endothelial dysfunction in T2D through increased release of ATP and myokines. In individuals with T2D we will determined blood flow in the muscle tissue using advanced ultrasound. In addition, using intravascular and intramuscular microdialysis we will determine ATP levels in blood and in the muscle interstitium.

NCT ID: NCT01993511 Recruiting - Obesity Clinical Trials

Changes in Glucose Metabolism After Roux-en-Y Gastric Bypass

Start date: June 2010
Phase: N/A
Study type: Observational

Besides causing weight loss Roux-en-Y gastric bypass (RYGB) has profound effect on glucose metabolism leading to remission of type 2 diabetes early after surgery. However the mechanisms for this improvement remain uncertain. The aim of this study is to investigate the changes in insulin sensitivity and beta-cell function 1 week and 3 months following RYGB using oral and intravenous test.

NCT ID: NCT01989364 Recruiting - Clinical trials for Uterine Cervical Neoplasms

Repetitive Functional Imaging in Locally Advanced Cervical Cancer

IMAP
Start date: January 2011
Phase: N/A
Study type: Observational [Patient Registry]

Background: The Apparent Diffusion Coefficient (ADC) acquired by Diffusion Weighted Imaging (DWI-MR) has been shown to correlate with cellular density. The ADC is indicative of Gross Tumour Volume (GTV), and preliminary data shows that the dynamics of DWI volumes during treatment (shrinkage) as well as dose to DWI volumes has impact on treatment outcome. Hypoxic tumour cells within the primary tumour have been identified to have prognostic importance for local control Tumour hypoxia is caused by insufficiency of the tumour vasculature leading to both chronic diffusion limited and acute flow limited hypoxia. Radioresistant hypoxic cells diminish the rate of local control, and the hypoxia driven increase in metastatic potential of the tumour and lowers the rate of distant disease control. Functional imaging has the potential to visualise radioresistant tumour subvolumes. PET scanning (18F-FAZA) is hypothesized to visualise hypoxic tumour subvolumes, and dynamic contrast enhanced (DCE) MR imaging has been used to quantify the extent of poor perfusion regions within cervical tumours. Objectives: Primary: Sensitivity and specificity of functional imaging (18F-FAZA PET (optional), T1w, T2w, DWI-MRI and DCE-MRI) to identify tumours with good and bad response to radio-chemotherapy Secondary: Determining whether there are differences in bias between centre. The difference in bias will be assessed for the T1 and T2 scans and the Ktrans and ADC maps.

NCT ID: NCT01988545 Recruiting - Healthy Clinical Trials

GLP-1's Effect on Cardiac Parameters and Mesenteric Blood Flow

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

to investigate the effect of the human incretin hormone GLP-1 on mesenteric blood flow and cardiac parameters

NCT ID: NCT01987882 Recruiting - Cerebral Palsy Clinical Trials

Cerebral Palsy Hip Outcomes Project - International Multi-centre Study

Start date: June 2014
Phase:
Study type: Observational [Patient Registry]

The primary purpose of the project is to evaluate the effectiveness of different intervention strategies to prevent or relieve symptoms associated with hip instability in children with severe cerebral palsy, using the validated Caregiver Priorities and Child Health Index of Life with Disabilities (CPCHILD©) questionnaire as the primary outcome measure of health-related quality of life for this population.

NCT ID: NCT01981213 Recruiting - Hepatic Injury Clinical Trials

Attempted Suicide With Acetaminophen Among 8-18 Year-old Children / Adolescents in Denmark

Start date: January 2005
Phase: N/A
Study type: Observational [Patient Registry]

A: Early predictors of hepatic injury after suicide attempt with acetaminophen: To explore the following in a pediatric population with acetaminophen overdose due to suicide attempt: 1) the prevalence of episodes of pre- and in-hospital vomiting and the relationship between the total number of vomiting episodes and hepatic injury, 2) the relevance of the early initiation of N-acetylcysteine (NAC) treatment to hepatic injury, and 3) the presence/absence of illness prior to the suicide attempt and hepatic injury. B: Characteristics, social behaviour, trends and risk factors: 1. To explore the relationship between children admitted to a paediatric department as a result of suicide attempts with acetaminophen and their parents and friends. 2. To determine the extent to which the children had attempted to speak to their parents or other adults about their problems before their suicide attempts. 3. To determine the prevalence of self-mutilation among children with suicidal behaviour. 4. To examine the reasons for these suicide attempts. C: Establishment of the expression of cytochrome P450 in a pediatric including the age-adjusted activities. Urine samples will be analyzed using an HPLC tandem mass spectrometric method, which we have already established in our lab. There will be categorized three groups for comparison: 1. An age-appropriate background population (approximately 200 patients) 2. Paediatric patients that have been admitted to Rigshospitalet, due to severe hepatic injury (approximately 50 patients) 3. Other pediatric patients admitted to their local hospital because of acetaminophen poisoning (approximately 200 patients) A control urine sample will be analyzed three months after the suicide attempt.

NCT ID: NCT01980134 Recruiting - Adenoma Clinical Trials

The MORDIS Study Clinical Investigational Plan

MORDIS
Start date: December 2013
Phase: N/A
Study type: Observational

To demonstrate the use of WavSTAT4 system during colonoscopy in identifying diminutive colorectal lesions (e.g. hyperplastic polyps) that can be resected and discarded (or even left in-situ) without adverse clinical impact.

NCT ID: NCT01979562 Recruiting - Overuse Injuries Clinical Trials

Knowledge of Predicting Increased Risk for an Overuse Injury in Runners

Start date: March 2014
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to examine the skeleton of the legs and the running style in order to predict a possible overuse injury.