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NCT ID: NCT02356458 Terminated - Clinical trials for Mantle Cell Lymphoma

Combination of Ibrutinib and Bortezomib to Treat Patients With Mantle Cell Lymphoma

Start date: August 31, 2015
Phase: Phase 1/Phase 2
Study type: Interventional

Mantle cell lymphoma (MCL) remains an incurable disease with frequent relapses and no standard therapeutic options in case of relapse. Prolongation of remissions or induction of longer remissions is therefore crucial. Recently, a synergistic increase in the proteasomal inhibition of ibrutinib in both bortezomib-sensitive and refractory MCL cells was shown. These findings, along with the reported single agent activities of both drugs and the non-overlapping toxicities, are the rationale to combine ibrutinib and bortezomib in MCL in this trial

NCT ID: NCT02354885 Recruiting - Bleeding Clinical Trials

TXA in the EMS on the Helicopter and the Ambulance

TXASRZREGA
Start date: December 2014
Phase: Phase 4
Study type: Interventional

Coagulopathy in trauma increases mortality and morbidity. Early administration of tranexamic acid (TXA) seems to improve survival and outcome. Thus this study evaluates the administration of TXA on scene by the emergency medical services (EMS) or by the crew of a rescue helicopter in multiple trauma patients or isolated traumatic brain injury (TBI). Coagulopathy will be assessed by standard laboratory tests as well as thromboelastometry.

NCT ID: NCT02353962 Completed - Hemispatial Neglect Clinical Trials

Evaluating the Feasibility and Usability of Exergames in Stroke Patients With Visuo-spatial Neglect

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

The aim of this study is to evaluate the feasibility and usability of newly developed exergames on exploring the hemineglected space of left neglected stroke patients. Furthermore to understand the experience of living with visuospatial neglect and to explore the users' experiences (patients and clinic staff) with those new exergames.

NCT ID: NCT02353949 Terminated - Dementia Clinical Trials

Investigating the Clinical Consequences of Flutemetamol-PET-scanning

Start date: May 2015
Phase: Phase 3
Study type: Interventional

The study examines subjects where there might be an indication for Amyloid-PET according to the Criteria defined by the Amyloid Imaging Task Force. In these subjects the impact of a Flutemetamol (Vizamyl)-Positron-Emission-Tomography -Scan (PET) on clinical management and disease course will be studied over 6 months.

NCT ID: NCT02353663 Completed - Clinical trials for Rheumatic Heart Disease

Rheumatic Heart Disease in Peru: Prevalence and Cardiovascular Outcomes Among Schoolchildren

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

Rheumatic heart disease remains a major challenge in low and middle income countries. Early detection of clinically silent valvular lesions by screening echocardiography allows timely implementation of secondary antibiotic prevention, and may prevent progression of disease to severe valvular damage and heart failure. The objective of the study is to assess the prevalence of rheumatic heart disease among schoolchildren in Arequipa, Peru. Subsequently, the investigators will evaluate progression of disease in children with early stages of subclinical rheumatic heart disease. The investigators will perform a population-based observational survey for rheumatic heart disease using portable echocardiography among schoolchildren aged 5 to 16 years from randomly selected public and private schools. Rheumatic heart disease will be documented both according to the modified World Health Organization definition and the echocardiographic criteria suggested by the World Heart Federation.

NCT ID: NCT02353585 Completed - Ischemic Stroke Clinical Trials

Novel Oral Anticoagulants in Stroke Patients

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

The present study will monitor and explore acute neurovascular emergencies in patients treated with NOACs compared to those under treatment with VKAs. The primary aims of this study are: (1) To investigate characteristics, management and outcome of intracranial hemorrhage (ICH) in patients treated with NOAC compared to VKA. (2) To investigate the management and outcome of patients with acute ischaemic stroke under NOAC compared to VKA.

NCT ID: NCT02353325 Completed - Iron Deficiency Clinical Trials

Iron Bioavailability From Encapsulated Ferrous Sulphate

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

Salt is one of the very few regularly purchased food item in all socioeconomic classes including poor remote areas with subsistence farming. Therefore, it is a promising vehicle for fortification with micronutrients, such as iodine, iron, vitamin A, to alleviate the burden of micronutrient deficiencies. However, ensuring the bioavailability of iron and the sensory quality in fortified salt is difficult. Water-soluble iron compounds, such as ferrous sulphate FeSO4, are the most bioavailable, but they react with moisture and impurities in salt, and cause unacceptable changes in colour. Encapsulation can reduce iron-mediated colour change in fortified salt without significantly compromise bioavailability. In the present project we aim to investigate the iron bioavailability from salt fortified with FeSO4 using a new encapsulation type based on hyaluronic acid (HA) and a polymer from the eudragit family (EPO).

NCT ID: NCT02351492 Completed - Gallstone Disease Clinical Trials

Radiological Investigation of Bile Duct Obstruction

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

Patients with gallstone disease should be checked whether a common bile duct (CBD) stone could be present. In case of a certain suspicion for CBD stones further investigations should be performed. This can either be done by magnetic resonance cholangio-pancreaticography (MRCP) or by intraoperative cholangiography. The study investigates which pathway would be favorable in regard of an early hospital demission.

NCT ID: NCT02350933 Completed - Intubation Clinical Trials

Endoscopic Evaluation of the Paediatric Airway After Prior Prolonged (>24 h) Tracheal Intubation

Start date: September 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether possible damages of the trachea caused by a prior prolonged intubation (> 24h) can be observed by rigid endoscopy of the trachea and if cuffed tracheal tubes cause less damages than cuffed tubes.

NCT ID: NCT02350907 Completed - Gonorrhoea Clinical Trials

Rapid Diagnosis of Antibiotic Resistance in Gonorrhoea

RaDAR-Go
Start date: February 2015
Phase:
Study type: Observational

The purpose of this study is to develop a laboratory-based assay that will be a real-time PCR test to detect the organism N. gonorrhoeae and its most important genetic markers of antimicrobial resistance. This study will also determine factors associated with gonorrhoea and describe sexual behaviours of men who have sex with men, to inform parameters for a mathematical model of gonorrhoea transmission and antimicrobial resistant gonorrhoea.