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NCT ID: NCT00511290 Completed - Asthma Clinical Trials

Measurement of Soluble Factors and Particulate Matter in Induced Sputum and EBC in Inflammatory Diseases of the Lung

Start date: n/a
Phase: N/A
Study type: Observational

In the present study inflammatory mediators will be isolated in induced sputum and exhaled breath condensate and will be correlated with particulate matter measured in these samples.Particulate matter will be assessed by partcle size distribution method and shape analysis. The aim of the study is to perform biological monitoring in environmental and occupational diseases in a non invassive fashion.

NCT ID: NCT00511589 Completed - Clinical trials for Protozoan Infections

Chagas Disease Diagnostic - Inconclusive Serology

Start date: n/a
Phase: N/A
Study type: Interventional

T. cruzi infection affects approximately five million people in Brazil. The diagnosis of the chronic phase of infection is performed by indirect serological methods which, nevertheless, leave inconclusive results. One of the direct methods used for T. cruzi identification, blood culture in LIT (liver infusion tryptose) medium, presents low sensitivity in that phase of the disease. A negative result does not eliminate the possibility of infection, but a positive test has high absolute diagnostic value, which enables the indication of antiparasitic treatment. Molecular diagnosis (PCR) in this phase is promising and can be used as a confirmatory test, particularly when individuals present inconclusive results in conventional serological tests, such as ELISA, HAI and IFI. This study aimed at improving blood culture sensitivity in LIT medium by performing PCR in individuals with positive and inconclusive serology for chagasic infection.

NCT ID: NCT00512811 Completed - Bronchiolitis Clinical Trials

Furosemide Inhalation in Dyspnea of Mustard Gas Exposed Patients

Start date: n/a
Phase: Phase 3
Study type: Interventional

to assess the efficacy of inhaled furosemide in mustard gas exposed patients with acute respiratory failure

NCT ID: NCT00513201 Completed - Diabetes Mellitus Clinical Trials

Lyspro Insulin vs Regular Insulin in Cirrhotic Patients

Start date: n/a
Phase: Phase 4
Study type: Interventional

OBJECTIVE: To compare lispro insulin and regular insulin in the glycemic control of patients with liver cirrhosis and type 2 diabetes subjects. METHODS: 108 patients with liver cirrhosis and type 2 diabetes were randomly treated with regular insulin or lispro. After 122 weeks a cross-over was carried out and patients followed-up for 122 weeks. Then, all patients received a standard breakfast of 145 kcal following 12 U.I. of regular insulin or lispro, and C-peptide and insulin serum levels were determined over 300 minutes.

NCT ID: NCT00514787 Completed - Asthma Clinical Trials

Be SMART NIS, Moderate to Servere Asthma Patient Observation

Start date: n/a
Phase: N/A
Study type: Observational

Screen for moderate to severe asthma patients with suboptimal asthma control (as defined by GINA-Guidelines). Document current asthma control status. Re-evaluate asthma therapy and document new therapy if applicable.

NCT ID: NCT00516594 Completed - Clinical trials for Cardiovascular Disease

The Effect of Altering Colonic Microflora After Fiber (FOS) Consumption

Start date: n/a
Phase: Phase 2
Study type: Interventional

Our antibiotic studies indicated that cholesterol lowering was seen when fecal bifidobacterial counts were increased. Due to the dangers associated with prolonged antibiotic use we have been funded by the Heart and Stroke Foundation to see if gut bacteria can be modified by non-antibiotic means. Inulin a dietary fiber found in artichokes, chicory, leaks, onion, etc., (which also produces flatulence) has been shown to increase bifidobacteria and also appears to lower serum cholesterol. We will therefore test the fiber to determine its effectiveness in lowering serum cholesterol and whether it can be used to maximize the cholesterol-lowering effects of soy protein foods and viscous fiber foods (e.g. oats and psyllium).

NCT ID: NCT00517413 Completed - Anemia Clinical Trials

LATINO Study: A Study of Mircera for the Maintenance Treatment of Dialysis Patients With Chronic Renal Anemia.

Start date: n/a
Phase: Phase 3
Study type: Interventional

This single arm study will assess the efficacy and safety of Mircera when administered once monthly, subcutaneously or intravenously, for the maintenance of hemoglobin levels in dialysis patients with chronic renal anemia. Patients currently receiving maintenance treatment with epoetin alfa will receive monthly injections of Mircera with a starting dose (120, 200 or 360 micrograms) derived from the dose of epoetin alfa they were receiving in the week preceding study start. The anticipated time on study treatment is 3-12 months, and the target sample size is 100-500 individuals.

NCT ID: NCT00518024 Completed - Tinnitus Clinical Trials

Safety and Effectiveness of Repetitive Transcranial Magnetic Stimulation in the Treatment of Tinnitus

Start date: n/a
Phase: Phase 2
Study type: Interventional

Tinnitus, i.e., the perception of sounds or noise in the absence of auditory stimuli, is a frequent and often severely disabling symptom of different disorders of the auditory system. There are currently no causal treatments. Using repetitive transcranial magnetic stimulation (rTMS), we have previously demonstrated that the temporoparietal cortex is critically involved in tinnitus perception and that tinnitus can be reduced by rTMS applied to these cortical regions. Therefore, it is reasonable to test rTMS as a potential new treatment strategy against tinnitus. At this stage, small pilot studies indicate some effect on tinnitus impairment but the reduction is predominantly reported to be transient, with high interindividual variability, and questionable clinical relevance. Moreover, the optimal stimulation area is unclear. Here, we use theta burst stimulation (TBS), a new rTMS paradigm for the prolonged modulation of cortical activity. The aim of this study is to test safety and effectivity of 4 weeks of daily bilateral TBS to two cortical areas on chronic tinnitus compared to sham-stimulation.

NCT ID: NCT00518700 Completed - Corneal Staining Clinical Trials

Comfort Evaluation of a New MPS vs. Replenish in Contact Lens Patients

Start date: n/a
Phase: Phase 4
Study type: Interventional

To compare corneal staining after contact lens instillation with a new MPS vs. RepleniSH

NCT ID: NCT00519948 Completed - Patient Comfort Clinical Trials

Comfort and Cleaning Evaluation of Multipurpose Solutions in Contact Lens Patients

Start date: n/a
Phase: Phase 4
Study type: Interventional

To compare patient comfort and overall lens cleanliness with consecutive use of two multipurpose lens solutions.