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Lung Disease clinical trials

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NCT ID: NCT01735526 Completed - Lung Disease Clinical Trials

Lung Diffusing Capacity for Nitric Oxide and Carbon Monoxide After Hematopoietic Stem-cell Transplantation

DLNO/DLCO
Start date: October 2012
Phase: N/A
Study type: Observational

Early after allogeneic hematopoietic stem-cell transplantation (allo-HSCT), reductions of absolute lung volume and diffusing capacity for carbon monoxide (DLCO) are frequently detected even in the absence of overt idiopathic pneumonia syndrome (IPS). It can be hypothesized that these changes might be due to an occult intersitial lung disease associated with infections, acute Graft-versus-Host Disease (aGvHD), myeloablative conditioning regimens or any combination of these. To test this hypothesis, we will simultaneously measure the lung diffusing capacity for nitric oxide (DLNO) and DLCO and estimate the changes of membrane diffusing capacity (DM) and pulmonary capillary volume (Vc) by the DLNO/DLCO ratio. As we hypothesize that GHVD should be intuitively absent amongst autologous HSCT (auto-HSCT) recipients, we will compare the changes in DLNO/DLCO ratio showed by the latter group with those of subjects undergoing allo-HSCT.

NCT ID: NCT01679301 Completed - Lung Disease Clinical Trials

Evaluation of Sleep Mode Within the Respironics SimplyGo Portable Oxygen Concentrator

Start date: September 2012
Phase: N/A
Study type: Interventional

The SimplyGo Study is a single site, cross-over study which aims to enroll a maximum of 30 participants (to allow for 20 completed data sets) with a prescription for nocturnal oxygen, and meeting all eligibility criteria.

NCT ID: NCT01404780 Completed - Lung Disease Clinical Trials

Comparison of the Glidescope and Macintosh Laryngoscope for Double Lumen Endotracheal Tube Intubation

Start date: June 2011
Phase: N/A
Study type: Interventional

Patients undergoing chest surgery often require insertion of a breathing tube (double lumen tube) after they are unconscious. The double lumen tube enables the anaesthetist to ventilate (assist breathing) one lung at a time. The other lung is partially deflated to enable enough space for the surgeon to perform the procedure. The breathing tube is inserted with a laryngoscope (blade with a light at the end) so the vocal cords can be seen. This is standard medical practise. Two laryngoscopes are commonly used at Toronto General Hospital to insert the tube. The Macintosh laryngoscope has been is use for over 50 years and the Glidescope for over 10 years. Both devices have been extensively researched for single lumen tubes insertion and found to be very safe and effective. Research is limited to say which of the two laryngoscope is the most effective for double lumen tubes.

NCT ID: NCT01289327 Completed - Lung Disease Clinical Trials

Propofol Versus Midazolam+Alfentanil for Sedation During Bronchoscopy: Comparison by Cutaneous Carbon Dioxide Tension

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

Although propofol is a popular agent for sedation during flexible bronchoscopy, some clinicians have raised concerns that it may cause greater respiratory drive reduction than more common drugs. However, this factor is difficult to accurately examine with pulse oximetry. The introduction of a novel device that noninvasively measures carbon dioxide (CO2) levels can help to resolve this controversy. The aim of this study is to evaluate the safety of conscious sedation with midazolam+alfentanil compared to propofol.

NCT ID: NCT01255592 Completed - Bronchiectasis Clinical Trials

Evaluation of the Effect of AZD5069 in Patients With Bronchiectasis

STRATUS
Start date: February 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate the effect of AZD5069 in patients with bronchiectasis.

NCT ID: NCT01222442 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

To Evaluate the Effect of AZD3199 on the Electrical Activity in the Heart

Start date: November 2010
Phase: Phase 1
Study type: Interventional

The purpose of this research study is to evaluate the effect of AZD3199 on the electrical activity of the heart. The effect of AZD3199 will be compared to a licensed antibiotic (moxifloxacin). Moxifloxacin effects on the electrical activity of the heart are well known. Safety and tolerability of AZD3199 and how much AZD3199 enters the blood circulation will also be assessed.

NCT ID: NCT01215279 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

AZD2423 Safety and Tolerability Study in Patients With Moderate and Severe Chronic Obstructive Pulmonary Disease(COPD)

Start date: October 2010
Phase: Phase 2
Study type: Interventional

The purpose of the study is to investigate the tolerability and safety of AZD2423 in Patients with chronic obstructive pulmonary disease.

NCT ID: NCT01184118 Completed - Lung Disease Clinical Trials

DREAM: Does Inhaled Fluticasone REsult in Obstructive Sleep Apnea Manifestations?

DREAM
Start date: March 2009
Phase: N/A
Study type: Interventional

This study is being conducted to find out if the use of inhaled corticosteroids has an affect on upper airway collapsibility and sleep apnea risk. An inhaled corticosteroid is a common asthma controller medication like Flovent. Sleep apnea is w hen someone stops breathing for a short period of time during sleep. For some reason, people with asthma have more sleep apnea and upper airway collapsibility (weakness) than the general population. There are many possible reasons for this and one might be related to the use of inhaled corticosteroids. The overall hypothesis of this study is to determine whether inhaled fluticasone propionate (FP) increases UAW collapsibility and to assess tongue (genioglossus muscle) dysfunction as a potential underlying mechanism.

NCT ID: NCT01153321 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Investigation of the Effect of Oral Treatment With 100 mg AZD2423 in Subjects With Mild Chronic Obstructive Pulmonary Disease (COPD)

Start date: October 2010
Phase: Phase 2
Study type: Interventional

The purpose of the study is to find out if AZD2423 can reduce inflammation in the lungs of patients with mild COPD.

NCT ID: NCT01107054 Completed - Pulmonary Disease Clinical Trials

A Study to Investigate the Effects of PF00610335 on the QT/QTC Interval in Healthy Volunteers

Start date: June 2010
Phase: Phase 1
Study type: Interventional

A study to determine the cardiovascular effects of PF00610335 in healthy volunteers.