Clinical Trials Logo

Filter by:
NCT ID: NCT01002976 Withdrawn - Clinical trials for Severe Allergic Asthma

Correlation Between IgE Parameters and the Response to Omalizumab in Subjects With Severe Asthma

OM-2009-XO
Start date: December 2009
Phase: Phase 4
Study type: Observational

Omalizumab is an anti-IgE recombinant humanized monoclonal antibody.The efficacy and tolerability of omalizumab have been demonstrated in patients with moderate-to-severe and allergic (IgE-mediated) asthma. Clinical benefit with omalizumab is observed when serum free IgE levels are reduced to 50 ng/mL or less. However, although the causal role of IgE in allergic disease is well established, the relationship between free IgE and clinical symptoms of asthma has not been accurately quantified. Recent study demonstrated that omalizumab and free IgE concentrations are correlated with clinical outcomes. In non responder to omalizumab the clinical symptoms show random fluctuations around baseline without any tendency toward improvement despite adequate suppression of free IgE. In these patients it may be the ratio of specific IgE to total IgE or inter-patient variability in the expression of FceRI on effector cells that define whether the patient will respond or not to omalizumab. This current study is designed to evaluate the mechanisms of responsiveness to omalizumab measuring the free IgE, specific IgE and the level of FceRI expression on the effector cell and the correlation to clinical response.

NCT ID: NCT00979355 Withdrawn - Clinical trials for Detect Pathalogical Lesions

Study to Compare a Fast Gama Camera for Nuclear Imaging to Conventional Camera

GP_D-Spect
Start date: November 2009
Phase: N/A
Study type: Interventional

A feasibility trial to evaluate the usefulness of a high efficiency camera (D-SPECT) as an imaging modality for general nuclear medicine applications such as oncology.

NCT ID: NCT00978809 Withdrawn - Clinical trials for Benign Paroxysmal Positional Vertigo

Effects of Physical Treatment on Postural Stability in Benign Paroxysmal Positional Vertigo (BPPV) Patients

Start date: September 2009
Phase: N/A
Study type: Interventional

The propose of this study is to compare two methods of physical treatment for benign paroxysmal positional vertigo, by evaluating treatment effects on postural stability. The trail design is a double blinded randomized controlled trail, with each patient going through three evaluations: before treatment, 1 week after treatment and 60 days after treatment.

NCT ID: NCT00973089 Withdrawn - Caries, Dental Clinical Trials

Alternative Treatment of Deep Carious Lesions Based on Biological Evidences

Start date: May 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the success rate of alternative treatment of deep carious lesions in asymptomatic primary teeth with no clinical nor radiographic signs of pulpal inflammation. The treatment includes leaving a thin layer of caries that is present near the pulp chamber and includes liner placement and tooth sealing. This alternative treatment is to be compared with the treatment provided today to these teeth, which includes complete removal of caries and probably includes pulpotomy and wide preparation of the tooth. The study also evaluates the cost-effectiveness of both methods of treatment of deep carious lesions.

NCT ID: NCT00956722 Withdrawn - Clinical trials for Asymptomatic Chronic HCV Carriers

Hyperimmune Bovine Colostrum - TRAVELAN™ for Patients With Chronic Hepatitis C Virus Infection Not Responding to Standard Therapy

Start date: January 2012
Phase: Phase 1
Study type: Interventional

This is an exploratory trial of Bovine Colostrum powder to decrease translocation of gut-derived microbial products and immune activation in HCV infection. The study is designed as a single-arm, open-label, before-and after exploratory trial of 10 weeks of Bovine Colostrum Powder (BCP) to reduce translocation of intestinal microbial products and immune activation in patients suffering from chronic hepatitis C virus (HCV) infection. The study population will include HCV-infected (genotype 1) men and women, ≥ 18 years of age, not receiving anti-viral therapy at the time of enrollment and for at least the previous 3 months. Having failed previous anti-viral therapy (non responders), HCV recurrence after 72 weeks of therapy, developed side effects which mandated stopping anti viral therapy, or not considered eligible for initiation of such treatment, with a plasma HCV RNA level ≥ 1000 I.U.

NCT ID: NCT00947037 Withdrawn - Parkinson's Disease Clinical Trials

Gastric Retentive Carbidopa/ Levodopa in Parkinson's Patients; a One Year, Open Label, Safety Extension Study

Start date: August 2012
Phase: Phase 2
Study type: Interventional

An extension of study IN 09 004 testing the long term safety of the Accordion Pill Carbidopa/Levodopa (AP-CD/LD)

NCT ID: NCT00937144 Withdrawn - Sickle Cell Anemia Clinical Trials

Endothelial Function in Patients With Sickle Cell Anemia Before and After Sildenafil

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

The investigators would like to study the endothelial function in sickle cell patients without pulmonary hypertension in an in vivo method during a steady state condition before and after sildenafil treatment for 1 month, and to study the effects of this nitric oxide donor by measuring the Flow Mediated Dilatation, by measuring endothelial progenitor stem cells colonies, and by measuring the effect of therapy on markers of inflammation (cell adhesion molecules and cytokines).

NCT ID: NCT00914836 Withdrawn - Bursitis Clinical Trials

Comparison of 2 Doses of Corticosteroid Subacromial Injections for the Treatment of Painful Shoulder

Start date: June 2009
Phase: N/A
Study type: Interventional

The use of corticosteroid subacromial injections have been found to be effective for the treatment of shoulder pain. Higher doses may be better than lower doses for subacromial corticosteroid injection for rotator cuff tendonitis. The investigators aim this study to compare 2 doses of corticosteroids.

NCT ID: NCT00907712 Withdrawn - Clinical trials for Diagnostic Techniques, Cardiovascular

Cardiovascular Assessment Before and After Limb Amputation

Start date: May 2009
Phase: N/A
Study type: Interventional

Vascular lower limb amputees have an increased morbidity and mortality. The aim of the study is to evaluate the hemodynamic changes after amputation and its relation to outcome.

NCT ID: NCT00905229 Withdrawn - Bleeding Clinical Trials

Comparing Different Routes and Doses of Phytonadione (Vitamin K) for Reversing Warfarin Treated Patients With Hip Fracture Before Surgery

Start date: May 2009
Phase: N/A
Study type: Interventional

It is well known that femoral neck fractures carry a significant increase in patients' mortality and that surgical intervention is the preferred treatment. Any delay in operating on such patients would inevitably increase their risk of developing complications. One of the reasons for such unintentional delay would be the hypercoagulative status of patients taking warfarin. The CHEST 2008 guidelines suggest reversing warfarin with Vitamin K for patients who need urgent operation. The aim of this study is to compare different roots and doses of Vitamin K.