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Dyspnea clinical trials

View clinical trials related to Dyspnea.

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NCT ID: NCT01461681 Completed - Depression Clinical Trials

Improving Care of Patients With Heart Failure

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

Heart failure (HF) affects more than 5 million Americans and is a major source of morbidity and mortality. Despite optimal management, over half of patients with HF suffer from pain, dyspnea, fatigue, and depression that diminish quality of life (QoL). HF care also exacts a huge financial toll with yearly costs of $35 billion. Although consensus guidelines call for providing palliative care (PC) to patients with HF to relieve suffering and improve QoL, few receive it. The overall aim of this project is to conduct a randomized controlled trial (RCT) to determine if an interdisciplinary PC intervention (Symptom Management Service-HF [SMS-HF]) provided concurrently with standard cardiology care improves symptoms, QoL and satisfaction, and reduces resource utilization in outpatients with Class II-IV HF compared to standard cardiology care alone. Subjects assigned to the SMS-HF group will receive a 6-month interdisciplinary PC intervention based on the investigators successful SMS model of outpatient PC for oncology patients and focused on assessment and management of physical, emotional, social, and spiritual distress and discussion of treatment preferences. Innovations of this study are that it will rigorously assess the impact of the SMS-HF on patient outcomes and on resource utilization, a key component to ensuring program sustainability. The investigators research team of PC and HF experts is recognized for its PC research and has a proven record of collaborating, conducting RCTs of PC interventions, and studying outpatients with HF. The environment at UCSF is highly supportive of innovative research and of sustaining programs with demonstrated improvements in patient outcomes and operational effectiveness. The overall goal is to use the results from this study to support an application to the NIH for a multi-center RCT of the SMS-HF and to study similar models of concurrent PC for patients with other serious illnesses.

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.

NCT ID: NCT01418248 Completed - Heart Failure Clinical Trials

Study of Exercise and Heart Function in Patients With Heart Failure and Pulmonary Vascular Disease

EXEC
Start date: August 2011
Phase: N/A
Study type: Observational

Heart Failure with Preserved Ejection Fraction (HFpEF) and Pulmonary Hypertension (PH) can be diagnosed noninvasively by Exercise Echocardiography (ExE) and Cardiopulmonary Exercise Testing (CPX) as compared with gold standard invasive hemodynamic assessment.

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: NCT01374880 Recruiting - Heart Failure Clinical Trials

Diagnostic and Prognostic Value of New Biomarkers in Patients With Heart Disease

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

The objective of this work is to investigate and then to sequence new biomarkers in the plasma of patients presenting with dyspnea secondary or not to heart failure, and study their diagnostic and prognostic value.

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.