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Dyspnea clinical trials

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NCT ID: NCT01615926 Terminated - Dyspnea Clinical Trials

Assessment of The Clinical Course of Dyspnea in Acute Heart Failure Patients

Start date: June 2012
Phase: N/A
Study type: Observational

Acute heart failure (AHF) is defined as a gradual or rapid change in heart failure (HF) signs and symptoms, such as shortness of breath (also called dyspnea or breathlessness), leg swelling, fatigue, breathlessness with exertion, trouble sleeping flat at night, and weight gain resulting in a need for urgent therapy. AHF results in over 1 million hospitalizations every year, resulting in an enormous public health burden. Approximately 1/3rd of patients will either be re-hospitalized or die within three months, and the resultant financial costs are large. As such, improving outcomes for AHF patients is critically important. Shortness of breath is the most common reason why patients with AHF present to the ER. As such, understanding how severe this symptom is, how much it improves with current treatments is very important to both patients and physicians. The purpose of this study is to determine the degree to which your shortness of breath improves during the first few days of hospitalization and its association with how fast you are breathing.

NCT ID: NCT01604655 Completed - Chest Pain Clinical Trials

ProspEctive First Evaluation in Chest Pain Trial

PERFECT
Start date: September 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the best initial test in patients admitted to the hospital complaining of chest pain.

NCT ID: NCT01601288 Completed - Dyspnea Clinical Trials

Database of All Patients Who Have Undergone Pulmonary Function Testing at Singapore General Hospital

Start date: May 2012
Phase:
Study type: Observational

The purpose of this study is to create a prospective database of all patients who have undergone pulmonary function testing from which the investigators can study the clinical phenotypes of various respiratory conditions. The investigators hope by understanding the differences in these myriad phenotypes to be able to provide individualized, patient-targeted therapy in the future.

NCT ID: NCT01585883 Completed - Lung Cancer Clinical Trials

Self-Management Intervention for Breathlessness in Lung Cancer

Start date: November 30, 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the suitability and practicality of a coaching and support intervention in helping patients to use daily strategies for managing breathlessness. Also, the investigators will try to understand how useful it is in helping patients to reduce intensity of breathlessness and its impact their quality of life.

NCT ID: NCT01580423 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

The Role of Substance P on Perception of Breathlessness During Resistive Load Breathing

SP-RLB
Start date: April 2012
Phase: N/A
Study type: Interventional

Substance P is released from sensory nerves and transmits pain information into the central nervous system. As pain and dyspnea share many characteristics, including similar neurological pathways, it is possible that substance P may contribute to the sensation of dyspnea. The hypothesis of the study is that patients with chronic obstructive pulmonary disease (COPD) will provide lower ratings of breathlessness during resistive load breathing with oral aprepitant, a medication that blocks the activity of substance P, compared with placebo.

NCT ID: NCT01577407 Completed - Pain Clinical Trials

Non Opioid Treatment for Experimental Dyspnea

Nefopel
Start date: September 2011
Phase: Phase 3
Study type: Interventional

The purpose of this protocol is to test the effects of the non opioid nefopam on experimental dyspnea and on the counterirritation (ie inhibition of one pain by another pain) induced by dyspnea in healthy subjects.

NCT ID: NCT01574066 Completed - Dyspnea Clinical Trials

Chest CT-scan for the Diagnosis of Community-acquired Pneumonia

PACSCAN
Start date: November 2011
Phase: N/A
Study type: Interventional

Primary objective : to estimate impact of CT-scan on diagnostic for emergency department (ED) patients with suspected Community-acquired Pneumonia (CAP). Secondary objective: to estimate impact of CT-scan on treatment (antimicrobial therapy) and site of care for ED patients with suspected CAP.

NCT ID: NCT01515566 Completed - Dyspnea Clinical Trials

Breakthrough Dyspnea Fentanyl Study in Cancer Patients

Start date: April 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if fentanyl given under the skin can reduce shortness of breath in cancer patients. Researchers also want to learn if it can help to improve your physical function. In this study, fentanyl will be compared to a placebo. Fentanyl is commonly used for treatment of cancer pain. It is believed to help patients with their shortness of breath as well. A placebo is not a drug. It looks like the study drug but is not designed to treat any disease or illness. It is designed to be compared with a study drug to learn if the study drug has any real effect.

NCT ID: NCT01510275 Completed - Dyspnea Clinical Trials

Combined Use of Respiratory Devices After Thoracic Surgery

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

In a rehabilitation setting, respiratory muscle training with re-expansion techniques in patients following cardio-thoracic surgery represents a consolidated intervention. New devices called RESPILIFT® and RESPIVOl® improve deep inspiration and pulmonary volume with an effect on respiratory muscle performance and perceived dispnoea. The aim of the investigators study is to test the clinical efficacy of RESPILIFT® and RESPIVOl® in patients with a recent history of cardio-thoracic surgery.

NCT ID: NCT01478932 Terminated - Dyspnea Clinical Trials

Diaphragmatic Breathing Retraining in Heart Failure Patients: Health-Behavior Related Outcomes

Start date: November 9, 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to provide information on how the practicing of diaphragmatic breathing retraining (DBR) for 8-week at home may improve the health outcomes and encourage heart failure patients to engage in health-promoting activities by successfully controlling their shortness of breath (dyspnea).