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NCT ID: NCT02364219 Recruiting - Hypothermia Clinical Trials

Impact of Prewarming on Perioperative Body Core Temperature and the Outcomes of Cytoreductive- and Major Open Abdominal Surgery: A Randomised Trial

PREWARM
Start date: February 2015
Phase: N/A
Study type: Interventional

The primary purpose of this study is to determine whether a prewarming period of at least 30 minutes during induction of general and combined epidural anesthesia reduces the core temperature drop normally occuring in patients undergoing cyto-reductive and major abdominal surgery. In addition the effect of prewarming on intra and postoperative body core temperature will be evaluated.

NCT ID: NCT02362126 Recruiting - Colorectal Adenomas Clinical Trials

Endoscopic Full Thickness Resection in the Lower GI Tract With the "Full Thickness Resection Device"

WALL-RESECT
Start date: February 2015
Phase: N/A
Study type: Observational

Observational prospective multicenter study to investigate efficacy and safety of endoscopic full thickness resection in the lower GI tract using a novel over-the-scope full thickness resection device.

NCT ID: NCT02361697 Recruiting - Clinical trials for Clinically Isolated Syndrome, CNS Demyelinating

DTI in Children With Multiple Sclerosis

Start date: December 2014
Phase: N/A
Study type: Interventional

This is a prospective, non-randomised, non-blinded, single center study of children and adolescents with multiple sclerosis and clinically isolated syndrome to detect differences or early changes in diffusion-weighted imaging (DTI) by magnetic resonance imaging (MRI).

NCT ID: NCT02361073 Recruiting - Clinical trials for Takotsubo Cardiomyopathy

The Role of Emotional Stress in Patients With Stress-induced Cardiomyopathy

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

The event-related potentials may be different in patients with Takotsubo cardiomyopathy than in patients without Takotsubo.

NCT ID: NCT02358720 Recruiting - Pain Clinical Trials

Single-fraction IMRT Versus External Beam Radiotherapy for Patients With Spine Bone Metastases

SMART
Start date: December 2014
Phase: Phase 1/Phase 2
Study type: Interventional

This study is a prospective, randomized, monocentre, controlled explorative study in the parallel-group design to determine the pain relief after RT of patients with spinal bone metastases. Thereby two different techniques were evaluated: single fraction IMRT with 1 x 24 Gy versus fractionated RT with 10 x 3 Gy. Prior to their enrolment into the study, the patients will undergo a staging of the vertebral column in connection with their radiation-planning computed tomography (CT) and MRI to measure the myelon dimension. After the baseline results have been recorded, the patients will be randomized into one of the two groups: single-fraction IMRT 1 x 24 Gy (n = 30) or fractionated RT 10 x 3 Gy (n = 30). The target parameters will be measured and recorded at baseline, at the end of RT (t1) and twelve weeks (t2) and six months following the end of the irradiation period (t3).

NCT ID: NCT02355457 Recruiting - Clinical trials for Myocardial Infarction

Biomarkers in Acute Cardiac Care

BACC
Start date: July 2013
Phase:
Study type: Observational [Patient Registry]

The primary aim of the study is to investigate new cardiac biomarkers and algorithms to diagnose acute coronary syndrome in patients with suspected acute myocardial infarction.

NCT ID: NCT02353533 Recruiting - Adenoma Clinical Trials

Endoscopic Full-thickness REsection of Residual Colorectal Lesions - The FiRE Study

FiRE
Start date: January 2015
Phase: N/A
Study type: Interventional

Adenomatous lesions of the colon are premalignant lesions which have the potential to develop cancer. Therefore adenomas should be resected endoscopically (endo- mucosa resection, EMR). EMR is conducted after submucosal injection of saline which allows to lift the desired lesion prior to resection. In some cases EMR is complicated due to incomplete or failed lifting after the injection of saline. This so- called "non- lifting" sign is a predictor for malignancy of the lesion. Difficult- to- lift polyps are also difficult- to- resect. A higher proportion of these lesions fail to be resected completely using the EMR technique. Alternatively, an over- the- scope full- thickness resection device (FTRD) can be used in order to resect colonic lesions. The FTRD technique has been described elsewhere (Schmidt et al. Gastroenterology 2014; 147: 740-742.e2). No comparative data exists until now on the performance of FTRD resection compared to standard EMR resection of difficult- to- resect colon adenomas. In this study the investigators aim to compare the success of FTRD versus EMR of difficult- to- resect adenomatous lesions (≤ 20 mm).

NCT ID: NCT02353455 Recruiting - Clinical trials for Adverse Reaction to Drug

Cells of Monocytic Origin as Surrogate Markers for Individual Drug Effects and Hepatotoxicity

Start date: March 2013
Phase:
Study type: Observational

Drug metabolism in the liver is subject to large fluctuations (differences between women and men, people of different ethnic backgrounds, children and adults). These large differences are responsible for very different drug effects and side-effects (and especially liver damage caused by drugs) between individuals. Recent scientific findings suggest that blood derived cells can be used to model individual effects of drugs on the liver reflect inter-individual differences. Since liver damage caused by drugs is a diagnosis of exclusion, the aforementioned cells can be used to identify patients that show higher sensitivity to hepatotoxic side-effects and - in case several drugs are involved - identify the causal agent or possible interactions.

NCT ID: NCT02352792 Recruiting - Clinical trials for Squamous Cell Carcinoma of the Head and Neck

Hypoxia-based Dose Escalation With Radiochemotherapy in Head and Neck Cancer

Start date: December 2008
Phase: N/A
Study type: Interventional

Patients with locally advanced suqamous cell carcinoma of the head and neck region receive a hypoxia scan either by magnetic resonance tomography, computed tomography or fluoromisonidazole (FMISO)-PET-CT. Patients presenting with hypoxia are randomized into standard therapy consisting of intensity modulated radiotherapy (IMRT) with 70 Gy plus either 5-fluorouracil/mitomycin C or cisplatinum (Arm A) or a dose escalation of 10% (77Gy) to the hypoxic volume applied via simultaneous integrated boost in addition to the standard treatment (Arm B).

NCT ID: NCT02350946 Recruiting - Clinical trials for The Impact of Oxytocin on Social Cognition

Effects of Oxytocin on Emotion Recognition and Response Inhibition

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

The purpose of this study is to shed light on the basic neurobiological mechanisms which underlie social information processing in healthy men. More specifically, we intend to examine whether a person's social competence level is related to the patterns of neural activity and his visual search strategies during evaluation of social scenes. Furthermore, it will be assessed whether an oxytocin-driven increase in activity in brain areas relevant to the task will facilitate social information processing and thus enhance task performance. Additionally it will be examined whether oxytocin can facilitate response inhibition in an emotional context.