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Dyspnea clinical trials

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NCT ID: NCT04090671 Active, not recruiting - COPD Clinical Trials

Evaluation of the Multidimensional Dyspnea Profile (MDP)

Start date: December 19, 2018
Phase: N/A
Study type: Interventional

Aim of this multicenter prospective cohort study is the evaluation of the multidimensional qualities of dyspnea in a number of diseases using the Multidimensional Dyspnea Profile (Banzett et al, ERJ 2015).

NCT ID: NCT03640455 Active, not recruiting - Dyspnea Clinical Trials

Randomized Study Evaluating the Efficacy of Low Intensity Transcranial Electrical Stimulation (Tdcs) for the Relief of Dyspnea

tDCS-DYSP-REA
Start date: November 9, 2018
Phase: Phase 2
Study type: Interventional

Nearly half (47%) of patients with mechanical ventilation in the intensive care unit report having dyspnea. This respiratory distress, with a feeling of "thirst for air", often reaches unbearable limits and is a major factor in the deterioration of the quality of life and the prognosis of patients. Physiopathological mechanisms of dyspnea are beginning better understood and have analogies with those of pain. Like pain, dyspnea often persists despite appropriate treatment of the cause, because of perceptual dysfunction related to changes in cortical excitability and neuronal plasticity and requires specific treatments. Studies have shown that Transcranial Stimulation by low Current (tDCS) was able to modulate the perception of acute pain induced and chronic pain. The tDCS modulates the functioning of a whole set of brain structures including the anterior cingulate gyrus, the prefrontal cortex, the thalamus and the brain stem, some of which have an established role in the central integration of pain and dyspnea. The investigators have recently demonstrated that the application of tDCS on the primary cortical motor area reduces the excitability of the central neurological pathways dedicated to the respiratory muscles in healthy subjects. The investigators therefore hypothesize that tDCS could relieve dyspnea in intensive care. In this research project, the investigators propose to evaluate the efficiency of tDCS on dyspnea in patients admitted to intensive care unit, having sepsis and mechanically ventilated.

NCT ID: NCT03604822 Active, not recruiting - Dysphagia Clinical Trials

Music Therapy Protocol to Support Bulbar and Respiratory Functions in ALS

Start date: September 27, 2017
Phase: N/A
Study type: Interventional

This study evaluates potential of music therapy treatment to support breathing, speech, swallow and cough of persons with amyotrophic lateral sclerosis (ALS). Music therapy is the clinical use of music and its elements to enhance human health and wellbeing. Application of music therapy principles in neurorehabilitation allow to treat cognitive, sensory, and motor dysfunctions.

NCT ID: NCT03367156 Active, not recruiting - Dyspnea Clinical Trials

Dexamethasone in Controlling Dyspnea in Patients With Cancer

Start date: December 4, 2017
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well dexamethasone works in controlling dyspnea in patients with cancer. Dexamethasone may help control dyspnea (shortness of breath) and improve lung function and quality of life in cancer patients.

NCT ID: NCT02357134 Active, not recruiting - Dyspnea Clinical Trials

High-Flow Oxygen in Reducing Shortness of Breath Caused by Exercise in Patients With Cancer

Start date: March 17, 2015
Phase: Phase 2
Study type: Interventional

This randomized phase II trial studies how well high-flow oxygen works in reducing difficulty breathing during exercise (exertional dyspnea) in patients with cancer. Dyspnea is linked to decreased lung function, quality of life, and survival. High-flow oxygen is a device that delivers heated and humidified oxygen through the nose. This may be effective in reducing dyspnea, and may help patients' lungs function better and improve their quality of life.

NCT ID: NCT02114944 Active, not recruiting - Dyspnea Clinical Trials

Treatment of Dyspnea in Do-not-intubate Patients

Start date: April 2014
Phase:
Study type: Observational

Patients with severe chronic diseases are often admitted to the hospital complaining of shortness of breath. Some of these patients decide that they do not want placement of a breathing tube in the windpipe to assist their breathing. In this situation, these patients are treated with oxygen, a variety of medications like morphine or masks that are connected to breathing machines, something called bilevel positive airway pressure (BiPAP) or noninvasive ventilation (NIV), to help with their breathing. Not much is known about how much noninvasive ventilation helps these patients, especially how comfortable they feel with it and how much their families think it helps. Our aim is to monitor use of ways to help breathing in patients who don't want a breathing tube, see how often noninvasive ventilation is used and ask surviving patients, patient's families and caregivers about their experience with noninvasive ventilation and how much it seemed to help. With our findings, we hope to improve the use of noninvasive ventilation in these patients and come up with ways to relieve their shortness of breath and provide as much comfort as possible.

NCT ID: NCT02007486 Active, not recruiting - Heart Failure Clinical Trials

Pathophysiological Mechanisms of Activity-Related Dyspnea in Heart Failure: A Pilot Study

Start date: January 2014
Phase: N/A
Study type: Observational

Dyspnea (breathlessness) on exertion is the most prevalent and distressing symptom of heart failure (HF). Nevertheless, the mechanisms of dyspnea in HF remain poorly understood. Thus, the general aim of this pilot study is to advance our understanding of the mechanisms of activity-related dyspnea in patients with HF. Studies will be performed in patients with mild, moderate and severe HF (n=24) as well as in healthy, age- and sex-matched control subjects (n=8). We will test the hypothesis that the increased prevalence and severity of activity-related dyspnea in HF reflects the interaction between an exaggerated drive to breathe and the inability of the respiratory system to meet this increased demand. Detailed physiological and perceptual responses to bicycle exercise will be examined and compared, first, between HF patients and healthy control subjects and, second, across patients with varying degrees of HF severity. The results from this preliminary study will be used to help design future studies in this patient population.

NCT ID: NCT01831115 Active, not recruiting - Dyspnea Clinical Trials

Basics in Acute Shortness of Breath EvaLuation (BASEL V) Study

BASEL V
Start date: April 2006
Phase:
Study type: Observational

To improve the diagnostic and prognostic utility of various biomarkers, detailed patient's history, physical examinations and technical devices in patients presenting with acute dyspnea.

NCT ID: NCT01452932 Active, not recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Muscle Training Effectiveness in the Degree of Dyspnea and Aerobic Capacity in COPD

Start date: June 2010
Phase: Phase 1/Phase 2
Study type: Interventional

Objective: To estimate the effectiveness of muscle training, the degree of dyspnea and aerobic capacity in patients over 50 with COPD, in a health care institution provider in Antioquia. Question: What is the effectiveness of muscle training, in the degree of dyspnea and aerobic capacity in COPD patients over 50 years, in a health service institution provider in the department of Antioquia? Hypothesis: Muscle training causes changes in the degree of dyspnea and aerobic capacity, other than the breathing exercises and relaxation Design: Randomized clinical trial with allocation and blinding of the autcomes assesor. Participants: COPD patients stage II and II, male and female, over 50 years old, who are attending to a community health service provider in the department of Antioquia. Intervention: A physiotherapeutic intervention using PNF technique was applied to the experimental physiotherapy group versus Yoga sessions applied to the other group. Twelve weeks protocol performing three sessions per week. Outcome measures: Dyspnea degree and aerobic capacity was measured using the MMRC scale and the six minute walking test respectively at the begining and the end of the study.

NCT ID: NCT01440764 Active, not recruiting - Healthy Clinical Trials

Aerosol Inhalation Treatment for Dyspnea

Start date: September 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this protocol is to develop and test optimal delivery of aerosol furosemide, a treatment that has the potential to significantly improve symptom management and enhance the quality of care for patients with intractable dyspnea.