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NCT ID: NCT01686425 Recruiting - Clinical trials for Malignant Biliary Obstruction

Percutaneous Transhepatic Cholangiography Versus Endoscopic Ultrasound Guided Biliary Drainage

PETRUS
Start date: July 2012
Phase: N/A
Study type: Interventional

Patients with obstructive jaundice due to locally advanced/metastatic malignancy with dilated intrahepatic bile ducts will be recruited from the department of Gastroenterology and Hepatology at the University Hospital of Leuven. This population will have failed ERCP or will be considered when ERCP is not possible due to altered surgical anatomy. Patients will be randomized to either PTC or EUS guided biliary drainage

NCT ID: NCT01673295 Recruiting - Lupus Nephritis Clinical Trials

RING - Rituximab for Lupus Nephritis With Remission as a Goal

RING
Start date: November 2014
Phase: Phase 3
Study type: Interventional

OBJECTIVE To test whether Rituximab (RTX) is efficacious to achieve complete renal response (CR) in Lupus Nephritis (LN) patients with persistent proteinuria (≥1g/d) despite at least 6 months of standard of care (SOC). STUDY DESIGN Investigator-initiated randomized international open multicentric 104-week study.

NCT ID: NCT01671540 Recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Effects of IPV Assessed With Functional Imaging

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

In this study the invetigators seek an answer on the following hypothesis: - What are the long term effects of an IPV treatment evaluated with classical outcome parameters? (FEV1, Raw) - Is the possible effect noticeable on the novel technique and is this comparable with the classical outcome parameters?

NCT ID: NCT01658956 Recruiting - Breast Cancer Clinical Trials

Effectiveness of Reduced GCSF Dosing in Patients With a Low to Moderate Risk of Febrile Neutropenia

PAPALDO
Start date: July 2012
Phase: Phase 2
Study type: Interventional

The study aims to confirm that a reduced dosage of GCSF is effective in preventing febrile neutropenia among patients with breast cancer, treated with chemotherapy and presenting with a low to moderate risk of developing febrile neutropenia.

NCT ID: NCT01657734 Recruiting - Malignant Gliomas Clinical Trials

Multimodal MR Imaging in Patients With Glioblastoma Treated With Dendritic Cell Therapy

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

Malignant gliomas are aggressive tumours with poor prognosis despite the current multimodal treatment. Hence, there is a clear need for new, effective therapies, among which immune therapy has emerged as a promising treatment option. When interpreting follow-up magnetic resonance (MR) examinations, the radiologist is often confronted with images that are difficult to interpret with the conventional anatomical imaging techniques. The difference between tumour relapse and therapy-mediated changes is not always distinctive. In this project, the investigators attempt to characterize the inflammatory response with parameters from advanced MRI techniques like MR spectroscopy, MR perfusion imaging and MR-diffusion imaging. These techniques allow characterization of cellular properties like metabolism and tissue structure respectively. Doing so, the investigators will monitor disease evolution in order to timely detect treatment failure, thereby allowing appropriate switch in patient management.

NCT ID: NCT01638130 Recruiting - Clinical trials for Brain Neoplasms, Primary Malignant

Experiences and Needs of Patients With a High-grade Glioma and Their Caregivers

Start date: February 2011
Phase: N/A
Study type: Observational

The purpose of this study is to explore the experiences and needs of patients with a high-grade glioma and their caregivers. Semi-structured interviews with patients and caregivers will be conducted and analysed using Grounded-Theory approach.

NCT ID: NCT01633489 Recruiting - Clinical trials for Lysosomal Acid Lipase Deficiency

Lysosomal Acid Lipase (LAL) Deficiency Registry

ALX-LALD-501
Start date: December 31, 2012
Phase:
Study type: Observational [Patient Registry]

This is an observational, multi-center, international disease registry designed to collect longitudinal data and create a knowledge base that will be utilized to improve the care and treatment of patients with LAL Deficiency. Participation in the Registry by both physicians and patients is voluntary.

NCT ID: NCT01618890 Recruiting - Liver Cirrhosis Clinical Trials

Hepatic Venous Pressure Gradient-guided Versus Standard Beta-blocker Therapy in Primary Prevention of Variceal Bleeding

Porthos
Start date: September 2012
Phase: Phase 3
Study type: Interventional

Study hypothesis: Hepatic venous pressure gradient (HVPG)-directed primary prophylaxis with nonselective beta-blocker therapy (NSBB) leads to a reduction in first variceal bleeding episodes and is cost-effective in the long term. Study design: A multi-center randomized controlled study comparing nonselective beta-blocker therapy guided by the hemodynamic response as determined by the difference in HVPG before and after starting oral NSBB therapy, to standard heart rate-guided NSBB therapy in patients with esophageal varices due to liver cirrhosis without a history of esophageal variceal hemorrhage. Primary study parameters/outcome of the study: First variceal bleeding episodes occurring within the first two years. Secondary study parameters/outcome of the study: - Mortality - Occurrence of other cirrhosis-related complications - Occurrence of hepatocellular carcinoma - Costs of treatments - Adverse effects

NCT ID: NCT01617382 Recruiting - Clinical trials for Peritoneal Carcinomatosis

Register With Patients in Which Hyperthermic Intra-Peritoneal Chemotherapy (HIPEC) Was Performed

HIPEC
Start date: May 2012
Phase:
Study type: Observational

The purpose of this study is to register the follow-up data of patients who, because of a peritoneal surface malignancy, will undergo cytoreductive surgery and HIPEC.

NCT ID: NCT01600144 Recruiting - Data Collection Clinical Trials

Data Collection for CAD Evaluation

Start date: March 2012
Phase: N/A
Study type: Observational

Mammographical data collection (raw data) for CAD evaluation by VUCOMp software.