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NCT ID: NCT03090763 Recruiting - Aortic Aneurysm Clinical Trials

Role of Circulating MicroRNAs in Pathogenesis of Aneurysms of the Abdominal and Thoracic Aorta - Study "Micro AAA"

Start date: November 1, 2016
Phase: N/A
Study type: Observational

The objective of this study is to establish whether patients with aortic aneurysm, compared to general population, have higher levels of selected miRNAs and whether there is significant association between the level of miRNA in circulating blood and the size of the aortic aneurysm or the risk of its rupture.

NCT ID: NCT03049020 Recruiting - Clinical trials for Pelvic Organ Prolapse Recurrence

The Efficacy of Laparoscopic Sacrocolpopexy in the Treatment of Pelvic Organ Prolapse in Women With or Without Avulsion of the Levator Ani Muscle

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

Based on a prospective study, to evaluate how pre-operative pelvic floor status - the presence of injury to the musculus levator ani - may influence the results of laparoscopic sacrocolpopexy. The investigators hope to confirm or disprove the hypothesis that the presence of such injury increases the risk of post-operative prolapse recurrence

NCT ID: NCT03040063 Recruiting - Limb Ischemia Clinical Trials

Complex Endovascular Approach to Treatment of Patients With Aneurysm of Popliteal Artery

EVAR-P
Start date: August 1, 2016
Phase: N/A
Study type: Interventional

Use of endovascular techniques - implantation of a peripheral stent graft and a peripheral flexible stent to isolate the sac of the popliteal artery aneurysm from the circulation and subsequent topical application of a thrombolytic (rtPA) to restore patency of the lower leg blood stream - will lead to a comparable or better outcome in treatment of patients with the popliteal artery aneurysm and acute critical limb ischaemia, compared to currently prevailing use of surgical treatment.

NCT ID: NCT03033810 Recruiting - Hemodynamics Clinical Trials

FFR Versus iFR in Assessment of Hemodynamic Lesion Significance

FiGARO
Start date: January 2017
Phase: N/A
Study type: Observational

The study will compare two invasive methods (FFR -fractional flow reserve and iFR—instantaneous wave free ratio) for assessment of hemodynamic impact of coronary stenosis on myocardial perfusion. There is a very good correlation between these methods for the assessment of hemodynamic significance in a broad spectrum of lesions. However, this correlation decreases significantly near the cut off points for each method. The investigators will try to find possible explanations for these differences by detailed morphology assessment of coronary stenosis using optical coherence tomography (OCT), analysis of gene polymorphisms that play a role in vasodilatation, and by shear stress analysis. The head-to-head comparison between FFR and iFR is not simple, because there is no "gold standard" for assessment of hemodynamic significance. Studies comparing these methods have used hyperemic stenosis resistance (HSR). For this kind of measurement it is necessary to measure the speed of blood flow. This is usually done by a Doppler analysis of flow. Unfortunately, the Doppler signal can yield many artificial or erroneous indicators, and obtaining a good quality signal is frequently time-consuming. These are the reasons that HSR has not been used in routine practice. The investigators have developed a new console and software that can provide real time analysis of the Doppler signal. It allows us to easily measure HSR, and to differentiate between the FFR and iFR measures through intrabeat analysis of microvascular resistance (lowest microvascular resistance is an essential condition for proper pressure measurement). Using this tool, it is possible to automatically identify the point of lowest microvascular resistance during each cardiac beat. The pressure gradient can then be measured at that point. This approach can eliminate almost all uncertainties in assessment of the pressure gradient produced by coronary stenosis. This tool can potentially improve the existing methods used to precisely reveal a significant stenosis. This should increase the number of hemodynamic guided procedures.

NCT ID: NCT02967094 Recruiting - Clinical trials for Gastroscopy; Gastric Cancer

Mucolytic Solution Before Upper Endoscopy

Start date: November 2016
Phase: N/A
Study type: Interventional

Study was designed to evaluate efficacy of mucolytic solution ingested before upper endoscopy on visibility of gastric mucosa.

NCT ID: NCT02908919 Recruiting - Colonoscopy Clinical Trials

Impact of Time Intervals of Preparation on Quality and Tolerance of the Bowel Preparation

Start date: August 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine optimal time intervals for preparation before colonoscopy using different formulas.

NCT ID: NCT02867436 Recruiting - Type 1 Diabetes Clinical Trials

The Effect of Gluten-free Diet on New Onset Type 1 Diabetes (T1D)

Start date: March 2016
Phase: N/A
Study type: Interventional

The primary aim of this pilot study is to test whether gluten-free diet (GFD) instituted in children shortly after onset of Type 1 Diabetes (T1D) can decelerate the decline in beta cell function as compared to age matched controls. Primary objective of the trial is the change in C-peptide area under the curve measured by mixed-meal tolerance test (MMTT) between group on GFD and standard gluten-containing diet. Secondary objectives are: - Changes in immune parameters between gluten-free diet group and control group; - Differences in fecal microbiome between children on normal diet and children on GFD;

NCT ID: NCT02777736 Recruiting - Clinical trials for Diffuse Large B-cell Lymphoma

CNS Prophylaxis in Diffuse Large B-cell Lymphoma

CLSG-CNS-001
Start date: July 2015
Phase: Phase 3
Study type: Interventional

Comparison of cumulative incidence of CNS relapses in patients with diffuse large B-cell lymphoma with intermediate or high risk of CNS relapse treated with CNS prophylaxis: either with 2 doses of intravenous methotrexate 3g/m2 i.v.(arm A) or 6 doses of intrathecal methotrexate 12mg (arm B) and in patients with low risk of CNS relapse without CNS prophylaxis (arm C).

NCT ID: NCT02582645 Recruiting - Impacted Canine Clinical Trials

Closed Window vs. Open Window Technique in Management of Palatally Impacted Canines

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

In this investigation the investigators would like to find out which of two commonly used techniques of management of palatally impacted canines: closed-window (CWT) or open-window (OWT), produces more favorable outcome.

NCT ID: NCT02543112 Recruiting - Asthma Clinical Trials

A Long-term Access Programme for Subjects With Severe Asthma

Start date: August 3, 2015
Phase: Phase 3
Study type: Interventional

This is a Long-term Access Programme (LAP) which aims to support provision of mepolizumab, until it is commercially available, to eligible subjects with severe asthma who participated in a GSK-sponsored mepolizumab clinical study 200862 and 200363. Eligible subjects will initiate mepolizumab within a 6-month period following the individual subject's last scheduled visit in their preceding clinical study. For each subject benefit versus risk will be assessed throughout the study to support continued treatment with mepolizumab.