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Dyspnea clinical trials

View clinical trials related to Dyspnea.

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NCT ID: NCT01399541 Completed - Depression Clinical Trials

Recovery and Rehabilitation After Lung Cancer Surgery

Start date: October 2010
Phase:
Study type: Observational

The specific aims of this translational, interdisciplinary, multi-center, international research study with 300 Lung cancer patients are to: Aim 1 Explore how the patients experience the transfer between different locations and between different levels of care at the same location and how they experienced coming home. Aim 2 Explore lung cancer patients' symptoms, symptom clusters, and changes in symptoms and symptom clusters over time. Aim 3 Explore interaction between lung cancers patients' symptoms, symptom clusters, health related quality of life and social support.

NCT ID: NCT01378520 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Effect of Ketoconazole on Breathlessness

KetoRLB
Start date: June 2011
Phase: Phase 4
Study type: Interventional

Beta-endorphins, which are naturally occurring narcotic substances, have been shown to alter the perception of breathlessness. Oral ketoconazole, an antifungal antibiotic, increases blood levels of beta-endorphins. The study hypothesis is that oral ketoconazole will reduce ratings of breathlessness induced by resistive breathing loads.

NCT ID: NCT01377051 Completed - COPD Clinical Trials

Effect of Indacaterol Maleate in Chronic Obstructive Pulmonary Disease (COPD) on Lung Volume and Related Dyspnea

Start date: May 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether indacaterol maleate 300 micrograms (mcg) is effective in the acute treatment of COPD and in particular on reducing lung hyperinflation and dynamic volumes.

NCT ID: NCT01364181 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

The Impact of Udenafil on Exercise Capacity in Severe Chronic Obstructive Pulmonary Disease (COPD) Patients

Start date: March 2010
Phase: Phase 3
Study type: Interventional

Pulmonary hypertension (PH) is a serious complication of COPD which is associated with shorter survival, more frequent exacerbation, and increased use of health resources. There is no effective pharmacological treatment for COPD-associated PH. Therefore, the investigators wanted to evaluate the effect of udenafil, a phosphodiesterase- 5 (PDE-5) inhibitor, on exercise capacity of severe COPD patients.

NCT ID: NCT01345188 Completed - Dyspnea Clinical Trials

Ranolazine in Ischemic Cardiomyopathy

Start date: April 2011
Phase: Phase 4
Study type: Interventional

Patients with ischemic cardiomyopathy may continue to experience persistent chest pain and shortness of breath despite conventional medical therapy and/or revascularization. The purpose of this study is to determine the efficacy of taking Ranexa versus placebo in patients with ischemic (due to blockages) cardiomyopathy treated with optimal conventional medical therapy and/or percutaneous revascularization.

NCT ID: NCT01331187 Completed - Dyspnea Clinical Trials

Influence of Routinely Adding Ultrasound Screening in Medical Department

Start date: April 1, 2011
Phase: N/A
Study type: Interventional

Ultrasound (US) is widely used as a diagnostic tool in a hospital setting. In a medical department, diagnosis like heart failure or most kinds of heart diseases, hypervolemia, hypovolemia, pleural effusion, pericardial effusion, ascites, diseases in the gall bladder/bile tract, urine tract and venous thrombosis are common. US is the key diagnostic tool in these diagnosis, and on early diagnosis is crucial with respect to the patients well-being and inpatients workflow. 1. The aim is to study the clinical use of pocket-size US as a screening diagnostic tool in an medical department with respect to inpatients workflow and diagnostics. Method: Patients admitted (in certain preset periods) to Department of medicine will be randomized to routinely adding an ultrasound examination with pocket-size device by residents on call. Time to definitive diagnosis, time to definitive treatment and time to discard will be recorded. US findings will be validated against standard echocardiography, or standard US/CT/MRI performed at the Radiological department.

NCT ID: NCT01287429 Completed - Clinical trials for Congestive Heart Failure

Lung Ultrasound for Acute Dyspnea in Emergency Department

Start date: October 2010
Phase: N/A
Study type: Observational

Dyspnea is a frequent symptom in patients admitted to the Emergency Department (ED); discriminating between cardiogenic and non-cardiogenic dyspnea is a common clinical dilemma. The initial diagnostic work-out is often not very accurate in defining the etiology and the underlying pathophysiology. In the last years, lung ultrasound (US) has emerged as a useful real-time bedside diagnostic tool in the critical patient. The aim of this study was to evaluate the accuracy, reproducibility, and diagnostic impact of pleural and lung US, performed by emergency physicians at the time of patient first presentation to the ED, in identifying cardiac causes of acute dyspnea.

NCT ID: NCT01286181 Completed - COPD Clinical Trials

Device-guided Breathing for Shortness of Breath in COPD

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

Although drug therapies and pulmonary rehabilitation have greatly improved COPD symptoms, as many as 50% of patients with severe COPD have inadequately controlled dyspnea. Device-guided breathing is a behavioral intervention that guides respiratory rates into a therapeutic range; prolongation of the expiratory phase improves hyperinflation, the most significant driver of dyspnea in this population. Device-guided breathing, has no known side-effects, and may represent a cost effective adjunctive treatment for dyspnea in severe COPD.

NCT ID: NCT01227317 Completed - Pulmonary Embolism Clinical Trials

BIOmarkers of Dyspnea IN Emergency Room

BIODINER
Start date: April 2010
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the capacity of some novels biomarkers Procalcitonin (PCT), Midregional Proadrenomedullin (MR pro ADM), Midregional pro-atrial natriuretic peptide (MR pro ANP), Copeptin (CT pro arginine vasopressin), Pro endothelin to stratify the risk in severe dyspnea.

NCT ID: NCT01197586 Completed - Dyspnea Clinical Trials

Evaluation of Surfactant Protein B in the Differential Diagnostics of Dyspnea

Start date: October 2010
Phase: N/A
Study type: Observational

Establishing new biochemical markers in the differential diagnostics and risk stratification in heterogeneous patient collectives is becoming more and more important. The markers should be objective, reliable, reproducible, quick and cost effective as well as specific and sensitive. Concerning the differential diagnostics of "dyspnea", NT-pro-BNP plays the most important role for the evaluation of a cardiac origin. However, a corresponding biochemical marker for pulmonary stress is lacking. The aim of the study at hand therefore was the evaluation of surfactant protein B in the differential diagnostics of pulmonary and cardiac diseases.