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NCT ID: NCT01103349 Completed - Asthma Clinical Trials

BI 671800 in Asthmatic Patients on Inhaled Corticosteroids

Start date: April 20, 2010
Phase: Phase 2
Study type: Interventional

This is a 6 week study to assess the effect of BI 671800 in patients with asthma. It is a double blind, parallel arm trial testing the safety and efficacy of BI 671800. The main objective is to assess the effect on lung function. The study will also provide data on the pharmacokinetics of BI 671800.

NCT ID: NCT01103297 Completed - Clinical trials for Distal Radius Fractures

2.4 mm Variable Angle LCP Two-Column Volar Distal Radius

VALCP2010
Start date: June 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to is to evaluate the postoperative loss of reduction rate in patients with distal radius fractures treated using the 2.4 mm Variable Angle LCP Two-Column Volar Distal Radius Plate ®.

NCT ID: NCT01102712 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Bronchoscopic Thermal Vapor Ablation (BTVA) for Lung Volume Reduction

BTVA
Start date: November 2009
Phase: N/A
Study type: Interventional

To establish and confirm the safety and clinical utility of BTVA applied unilaterally for lung volume reduction in patients with upper lobe predominate heterogeneous severe emphysema.

NCT ID: NCT01102426 Completed - Clinical trials for Relapsed/Refractory Multiple Myeloma

Aplidin - Dexamethasone in Relapsed/Refractory Myeloma

ADMYRE
Start date: June 2010
Phase: Phase 3
Study type: Interventional

Study of Plitidepsin in combination with dexamethasone versus dexamethasone alone in patients with relapsed/refractory multiple myeloma.

NCT ID: NCT01099566 Completed - Healthy Volunteers Clinical Trials

The Role of the P2Y12 Receptor in Tissue Factor Induced Coagulation

Start date: November 2009
Phase: Phase 4
Study type: Interventional

Severe sepsis still carries a high mortality rate despite advantages in intensive care medicine and antimicrobial therapy. The inflammatory and procoagulant host response to infection are intricately linked and interactions between platelets, leukocytes and the endothelium play a central role in the pathogenesis of septic shock and disseminated intravascular coagulation (DIC). Interestingly, one key player cell in coagulation, i.e. the platelet, has been somewhat neglected as to its position in the pathogenesis of coagulation abnormalities in sepsis. However, thienopyridines, irreversible platelet P2Y12 ADP-receptor antagonists, e.g. prasugrel, could potentially provide beneficial anticoagulatory and antiinflammatory effects: P2Y12 ADP-receptor antagonists reduce TF-induced coagulation activation in various ex vivo and in vitro models. Moreover, various lines of evidence indicate that thienopyridines may block platelet leukocyte interactions and thereby reduce the propagation of the coagulation and inflammation process. LPS-infusion in healthy volunteers provides a standardized model to safely study non overt DIC and to document possible effects of therapeutic and prophylactic interventions. The investigators hypothesize that thienopyridines, irreversible platelet P2Y12 ADP-receptor antagonists, may blunt TF-triggered coagulation activation in humans, which will be studied in a TF-dependent coagulation model in humans.

NCT ID: NCT01098591 Completed - Clinical trials for Ischemic Heart Disease

Meta-Analysis of Cell-based CaRdiac stUdiEs: ACCRUE

ACCRUE
Start date: November 2007
Phase:
Study type: Observational

Numerous human cardiac stem cell studies have been published, including relatively small number of patients. Meta-analysis of randomized trials have reported safety and a 3-6% increase in global left ventricular performance after intracoronary stem cell therapy in patients with acute myocardial infarction. Since most of the studies used different type of stem cells, delivery modes, and patient population, the results are heterogenous, therefore the comparison of the results is biased regarding generalizable conclusions about the effect of treatment. The present comparative meta-analysis is based on individual patient data, and gathers and pools the raw data, and analyzes the clinical outcome, safety and efficacy of the cardiac stem cell therapy.

NCT ID: NCT01097174 Completed - Clinical trials for Open Angle Glaucoma (OAG)

CyPass Clinical Experience Study

CyCLE
Start date: December 2009
Phase: N/A
Study type: Observational

This study is to evaluate the long-term safety, effectiveness and clinical experience of the CyPass Micro-Stent in patients with glaucoma.

NCT ID: NCT01093664 Completed - Alzheimer's Disease Clinical Trials

Safety/Tolerability, Immunological and Clinical Activity of a Boost Immunization With AFFITOPE AD02

Start date: October 2009
Phase: Phase 1
Study type: Interventional

This is a phase IB follow-up study to assess a boost immunization with AFFITOPE AD02 with regard to safety/tolerability, immunological and clinical activity in Alzheimer patients who have received the vaccine within the clinical study AFF002.

NCT ID: NCT01093534 Completed - Overactive Bladder Clinical Trials

Study of 2 Doses of Solifenacin Succinate in Female Subjects With Overactive Bladder.

SHRINK
Start date: January 2010
Phase: Phase 4
Study type: Interventional

The purpose is to see if solifenacin has any effect on bladder wall thickness and urine inflammatory marker measurements after 12 weeks of treatment.

NCT ID: NCT01093326 Completed - Multiple Sclerosis Clinical Trials

Clinical Study to Investigate the Long-term Safety, Tolerability, and Efficacy of Ponesimod in Patients With Relapsing-remitting Multiple Sclerosis

Start date: May 12, 2010
Phase: Phase 2
Study type: Interventional

This study is an extension to the study AC-058B201 and will investigate the long-term safety, tolerability and efficacy of ponesimod in patients with relapsing-remitting multiple sclerosis.