Clinical Trials Logo

Filter by:
NCT ID: NCT02072863 Completed - Multiple Myeloma Clinical Trials

A Study of Oprozomib, Melphalan, and Prednisone in Transplant Ineligible Patients With Newly Diagnosed Multiple Myeloma

Start date: January 2014
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of Phase 1b of the study is to determine the maximum tolerated dose (MTD) of oprozomib in combination with melphalan and prednisone (OMP). The purpose of Phase 2 of the study is to estimate the overall response rate (ORR) and complete response rate (CRR) of the OMP combination.

NCT ID: NCT02072434 Completed - Atrial Fibrillation Clinical Trials

Edoxaban vs. Warfarin in Subjects Undergoing Cardioversion of Nonvalvular Atrial Fibrillation (NVAF)

ENSURE-AF
Start date: March 25, 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare edoxaban to warfarin (with enoxaparin, if needed). It will see if edoxaban prevents stroke and other blood clotting problems as well and as safely as warfarin. People with atrial fibrillation (irregular heartbeat) might be able to join. Their doctors must plan to use shock to make their hearts beat normally. About 2200 people from different countries will join. They will have an equal chance of receiving either treatment. They are anticipated to be in the study for around 82 days. Tests will include physicals and finger-pricks. Participants will provide blood and urine samples.

NCT ID: NCT02070991 Completed - Clinical trials for Pulmonary Hypertension

Clinical Study to Evaluate the Safety and Tolerability of Macitentan in Subjects With Combined Pre- and Post-capillary Pulmonary Hypertension (CpcPH) Due to Left Ventricular Dysfunction

MELODY-1
Start date: July 1, 2014
Phase: Phase 2
Study type: Interventional

Study to evaluate if macitentan is safe and tolerable enough to be used for treatment of subjects with combined pre- and post-capillary pulmonary hypertension (CpcPH) due to left ventricular dysfunction.

NCT ID: NCT02070731 Completed - Clinical trials for Aortic Valve Stenosis

DEFLECT III: A Prospective, Randomized Evaluation of the TriGuardâ„¢ HDH Embolic Deflection Device During TAVI

TAVI
Start date: February 2014
Phase: N/A
Study type: Interventional

A randomized evaluation of the TriGuardâ„¢ HDH embolic deflection device during transcatheter aortic valve implantation.

NCT ID: NCT02069899 Completed - Clinical trials for Hemophagocytic Lymphohistiocytosis

A Study for Long-term Follow-up of Hemophagocytic Lymphohistiocytosis (HLH) Participants Who Received Treatment With Emapalumab (NI-0501), an Anti-interferon Gamma Monoclonal Antibody

Start date: August 4, 2014
Phase: Phase 2/Phase 3
Study type: Interventional

International, multicenter, long-term, follow-up study that will enrol HLH participants who have received emapalumab in previous clinical trials, in the context of the clinical development program for emapalumab or under compassionate use (CU).

NCT ID: NCT02069639 Completed - Clinical trials for Hodgkin's Lymphoma Patients Who Underwent an Allogeneic Stem Cell Transplantation

TARC After alloSCT in Hodgkin's Lymphoma

TARC
Start date: November 2013
Phase: N/A
Study type: Observational

Relapsed and refractory Hodgkin's lymphoma (HL) patients may experience long-term survival after allogeneic transplant (alloSCT), but disease recurrence represents the main cause of treatment failure. PET (positron-emission tomography) -positive patients after alloSCT have a dismal outcome. Serum TARC (thymus and activation-regulated chemokine) is produced by Reed-Sternberg cells and may be a marker of disease. Our study was aimed at assessing whether TARC levels after alloSCT were correlated to disease status and whether TARC monitoring could increase the ability to predict relapse.

NCT ID: NCT02069561 Completed - Ulcerative Colitis Clinical Trials

Effects of Eicosapentaenoic Acid on Subjects at High Risk for Colorectal Cancer

EPAUC
Start date: January 2014
Phase: N/A
Study type: Interventional

The aim of this study is to test Eicosapentaenoic acid's effects on markers relevant to colorectal carcinogenesis, RNA and DNA profiles, and the possibility that Eicosapentaenoic Acid treatment might be associated with changes of the gut microbiota and metabolomic profiles in patients with long-standing ulcerative colitis.

NCT ID: NCT02068807 Completed - Clinical trials for Infant, Newborn, Diseases

Evaluation of Antioxidant Activity of Oral Lutein in Preterm and Term Newborn

Start date: January 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The balance of the redox state is important for normal embryonic and fetal development . During the perinatal period, a variety of conditions are responsible for an excessive production of free radicals. The following oxidative stress is exacerbated by a lack of antioxidant substances that have not yet matured. At the moment there are no therapeutic strategies with single or combined antioxidants that have been shown to be clinically effective. Breastfeeding is important for the contribution of the antioxidant defenses of the newborn and the nutritional status of the mother plays a key role because it influences the nutritional status of the newborn. Lutein is a carotenoid that is not produced by the body , but taken with food or supplements. The molecule carries out different activities : antioxidant, anti-inflammatory, anticancer , neuroprotective. Its main activity of inhibition of peroxidation of membrane lipids is peculiarly important for the photoreceptors and neurons whose membranes are rich with polyunsaturated fatty acids. Current evidence on its role as an antioxidant indicate that supplementation with lutein may play a significant role in the prevention of free radical disease in the newborn

NCT ID: NCT02068482 Completed - Clinical trials for Diverticular Disease

Immunohistology in USDD and Correlation Between Bacterial Flora and Phlogosis

Start date: November 2010
Phase: Phase 4
Study type: Interventional

Diverticulosis of the colon is a frequent condition in adults in western countries and a significant number of patients experience clinical symptoms even when the diverticulosis is not complicated by diverticulitis. Both central and mucosal immunity are altered in Uncomplicated Symptomatic Diverticular Disease (USDD) and Rifaximin ameliorate clinical symptoms and normalize the immunological abnormalities. The Study Protocol is verify the modifications in the immunological pattern induced by reducing bacteria related activation of immunity by Rifaximin treatment.

NCT ID: NCT02067143 Completed - Secondary Clinical Trials

MRD/Risk-oriented Therapy of Adult Ph- ALL Including Pegylated Asparaginase and Lineage-targeted Methotrexate

LAL1913
Start date: May 20, 2014
Phase: Phase 2
Study type: Interventional

This study will be conducted in different centres and will study adult patients with Philadelphia chromosome-negative (Ph-) acute lymphoblastic leukemia (ALL). The study treatment will include a induction/consolidation therapy incorporating pegylated Asparaginase (Peg-ASP) and lineage-targeted high-dose methotrexate plus other antileukemic drugs, for the achievement of an early negative minimal residual disease (MRD) status. The MRD study supports a risk/MRD-oriented final consolidation phase.