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NCT ID: NCT03299608 Recruiting - Clinical trials for Respiratory Tract Infections

Rapid Analysis of Infections by Spectrometry of Exhaled Breath

RAISE
Start date: June 21, 2019
Phase:
Study type: Observational

To quantify the diagnostic, prognostic and therapeutic value of spectrometric analysis of exhaled breath from hematological patients with respiratory infection.

NCT ID: NCT03299179 Recruiting - Contraception Clinical Trials

The Effects of the Female Hormones on Cerebral Perfusion

Start date: October 3, 2016
Phase:
Study type: Observational

Measuring brain perfusion is biased by a inter- and intrasubject variability, caused by physiological and lifestyle factors. In this study, the investigators want to investigate the variations in cerebral perfusion and other brain parameters (grey matter, resting-state brain activity, brain connectivity and white matter diffusion) caused by the female sex hormones and hormonal contraception.

NCT ID: NCT03296267 Recruiting - Clinical trials for Functional Dyspepsia

Influence of Bile Acids on Bacterial Uptake in Functional Dyspepsia

Start date: January 2, 2017
Phase: N/A
Study type: Interventional

In up to half of patients seen by gastroenterologists, routine examinations fail to find an underlying organic, systemic, or metabolic disease that readily explains the symptoms. These patients are referred to as patients with disorders of gastrointestinal function, of which functional dyspepsia (FD) is one of the most common. Despite intensive research to investigate various pathophysiological mechanisms of this disease, the pathogenesis remains obscure. The investigators recently demonstrated increased duodenal permeability in FD patients, as assessed by mounting routine endoscopic duodenal biopsy specimens into Ussing chambers to measure transepithelial electrical resistance and passage of a paracellular fluorescent probe. Impaired intestinal barrier function can lead to increased uptake of luminal substances which can induce an immunological response in the mucosa. Interestingly, using transmission electron microscopy (TEM) in duodenal biopsies, the investigators recently observed the presence of a yet to be identified microorganism inside the epithelium and the lamina propria of a subset of FD patients (unpublished observations), suggesting increased translocation of microorganisms. The aim of the project is to investigate whether FD patients display increased translocation of microorganisms in duodenal biopsies. The investigators will also test the effect of bile acid on translocation of microorganisms and therefore include 20 FD patients and 20 age- and gender-matched healthy volunteers in this study.

NCT ID: NCT03293017 Recruiting - Clinical trials for Alcohol Use Disorder

Baclofen in Managing Acute Alcohol Withdrawal

Start date: February 1, 2016
Phase: Phase 4
Study type: Interventional

The study goal is to investigate whether administration of oral baclofen forms an adequate treatment option in the management of acute alcohol withdrawal. The investigators will compare placebo with doses of baclofen 30 and 60 milligram per day (mg/day) in a randomized controlled trial including patients receiving symptom triggered diazepam.

NCT ID: NCT03277391 Recruiting - Thoracic Surgery Clinical Trials

Serratus Anterior Plane Block: Post-operative Analgesia in Video-assisted Thoracic Surgery

Serrathos
Start date: April 14, 2017
Phase: N/A
Study type: Interventional

The objective of the study is to compare the efficacy of the Serratus Anterior Plane block (SPB) realised in its deep plane, with a multi-holed catheter in place for twenty four hours, to a standard intravenous analgesia for small videoassisted thoracic surgery interventions. The objective is also to evaluate the resorption rate of local anesthetic at this level, and make a population pharmacokinetic analysis.

NCT ID: NCT03264768 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Endoscopic Long Volume Reduction by Endobronchial Valves in Belgium

BEVA
Start date: August 1, 2017
Phase: N/A
Study type: Interventional

This a single center non-randomised non-sham controlled intervention study evaluating the effectiveness and safety of endoscopic lung volume reduction by endobronchial valves

NCT ID: NCT03257033 Recruiting - Clinical trials for Locally Advanced Pancreatic Cancer

Intra-arterial Gemcitabine vs. IV Gemcitabine and Nab-Paclitaxel Following Radiotherapy for LAPC

TIGeR-PaC
Start date: March 12, 2018
Phase: Phase 3
Study type: Interventional

The study is a multi-center, un-blinded, randomized control study of subjects with locally advanced pancreatic adenocarcinoma which is unresectable.

NCT ID: NCT03256240 Recruiting - Crohn's Disease Clinical Trials

Study of the Kono-S Anastomosis Versus the Side-to-side Functional End Anastomosis

Start date: March 12, 2014
Phase: N/A
Study type: Interventional

This study proposes a randomized prospective study comparing the Kono-S anastomosis to the standard side-to-side anastomosis.This will be a multi-center randomized prospective trial. Patients with Crohn's ileitis or Crohn's ileocolitis requiring resection will be randomized to undergo either the Kono-S anastomosis or the side-to-side functional end anastomosis.

NCT ID: NCT03252795 Recruiting - Infertility, Female Clinical Trials

Uterus Transplantation From a Multi-organ Donor

Start date: November 3, 2016
Phase: N/A
Study type: Interventional

Uterus transplantation: screening, in vitro fertilization [IVF] treatment to be able to freeze embryos, uterus transplantation, pregnancy and afterwards removal of the uterus.

NCT ID: NCT03250000 Recruiting - Physical Activity Clinical Trials

Changes in Microcirculation and Functional Status During Exacerbation of COPD

COPD-EX
Start date: September 8, 2017
Phase: N/A
Study type: Observational

This study investigates the influence of acute exacerbation of chronic obstructive pulmonary disease (COPD) on retinal microcirculation, on functional status and also investigates the prognostic value of retinal vessel caliber assessment in terms of hospitalization and mortality during 2 years of follow-up.