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Cough clinical trials

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NCT ID: NCT01854268 Completed - Cough Clinical Trials

Respiratory Kinematics During Voluntary and Reflex Cough in Healthy Adults

Start date: May 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Cough is a defensive behavior that involves three stages. A large inspiratory phase, a compression phase where the vocal folds close and subglottal pressure is developed, and an expiratory phase. Cough serves to protect the upper and lower airways from material such as liquids, solids, or saliva, that have been aspirated. There are two types of cough: voluntary and reflex cough. Voluntary cough involves a cough to command. Reflex cough is a cough that is generated secondary to a stimulus in or near the airway. There has been some research regarding the differences between voluntary and reflex cough. However, no research has described the differences in airflow or movement pattern (kinematics) between the two types of cough. This study seeks to determine the respiratory kinematics and airflow differences between voluntary and reflex cough in healthy participants.

NCT ID: NCT01807832 Not yet recruiting - Chronic Cough Clinical Trials

The Use of Capsaicin Challenge for Diagnosis, Monitoring and Follow-up of Chronic Cough.

Start date: March 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the capsaicin challenge can improve the diagnosis, treatment, monitoring and follow-up in patients with chronic cough.

NCT ID: NCT01777867 Completed - Clinical trials for Gastroesophageal Reflux Disease

Cough Reflex Sensitivity and Bronchial Hyper-responsiveness

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

The aim of this study is to provide pilot data on the possible gastrointestinal predictors of respiratory hyper-responsiveness and how these relate to the clinical sub-types of gastroesophageal reflux disease (GERD) and visceral acid hypersensitivity.

NCT ID: NCT01774292 Completed - Lidocaine Clinical Trials

Effect of Intracuff Alkalinized Lidocaine on Coughing Incidence at Extubation

Start date: January 2013
Phase: Phase 4
Study type: Interventional

The purpose of the study is to determined whether the administration of alkalized 4% lidocaine (160 mg) in the endotracheal tube cuff is effective in diminishing the incidence of coughing at extubation in surgeries lasting more than 2 hours without the use of nitrous oxide as an anesthetic agent.

NCT ID: NCT01738711 Not yet recruiting - Clinical trials for Idiopathic Pulmonary Fibrosis

Does CBT Improve the Perception/Impact of Cough and Breathlessness in IPF Patients

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

Idiopathic Pulmonary Fibrosis (IPF) is a chronic progressive lung disease of unknown cause for which there is no effective medical treatment. The main symptoms are increasing breathlessness and cough which can significantly impact on quality of life (QOL) often leading to anxiety and depression. The focus of disease management is shifting from pharmacological attempts to reduce disease progression to managing symptoms and a more holistic approach. Cognitive behavioural therapy (CBT) is increasingly used to treat anxiety and depression in chronic disease. Our investigators aim to determine whether CBT can reduce anxiety and depression related to symptoms and improve QOL in patients with IPF. This study will compare CBT intervention (Group 1) against standard treatment (Group 2). Patients will be recruited from a specialist IPF clinic - all patients attending with IPF who suffer from anxiety will be eligible to participate in the study. The study aims to recruit 30 patients (15 in each group). Patients will be randomly allocated into each group using an envelope concealment system. At entry a baseline visit will be conducted with information gathered regarding disease severity, hospital admissions, medication, symptoms (subjective and objective), quality of life and anxiety and depression using questionnaires and routine clinical tests. Patients will then receive CBT intervention (Group 1) or no intervention (Group 2). Patients receiving CBT will undergo a maximum of 6 (minimum of 2) individual therapy sessions. Follow up visits for both groups will be conducted at 3, 6, 9 and 12 months with the same information gathered as at the baseline visit.

NCT ID: NCT01735084 Completed - Cough Clinical Trials

Using Pneumococcal Vaccines in Combination for Maximum Protection From Ear and Lung Infections in First 3 Years of Life

PREV-IX_B
Start date: March 12, 2013
Phase: Phase 4
Study type: Interventional

HYPOTHESES: 1. That infants receiving PHiD-CV10 as a booster at 12 months of age, compared to controls having no PHiD-CV10 booster (i.e. standard PCV13), will have higher HiD antibody levels, lower carriage of NTHi, and less tympanic membrane perforation at 18 and 36 months of age. 2. That infants receiving PCV13 as a booster at 12 months of age, compared to controls having no PCV13 (i.e. PHiD-CV10 booster) will have higher antibody levels to serotypes 3, 6A and 19A, less carriage of these serotypes, and less tympanic membrane perforation at 18 and 36 months of age.

NCT ID: NCT01721395 Completed - Cough Clinical Trials

Effect of Agave Syrup, Placebo, and No Treatment on Nocturnal Cough and Sleep Quality for Coughing Infants/Toddlers and Their Parents

Start date: January 2013
Phase: N/A
Study type: Interventional

Cough is a frequent symptom in children and infants and is one of the most common reasons parents visit a healthcare provider for their child. The US Food and Drug Administration has issued a warning that over-the-counter cough and cold medicines including antihistamines, decongestants, anti-tussives, and expectorants should not be administered to children younger than 2 years of age due not only to lack of proven efficacy, but also because of important safety concerns. Honey, another method of soothing cough cannot be used in children <1 year due to concerns for infantile botulism. A preparation from agave syrup has been created to address the need for an infant cough syrup. Although no studies have formally evaluated the use of agave nectar for nocturnal cough associated with Upper Respiratory Infections, the demulcent effect and sweet taste of agave nectar may provide some relief from cough in children.

NCT ID: NCT01715688 Completed - Anesthesia Clinical Trials

Efficacy of Alkalinized Lidocaine in the Endotracheal Tube Cuff on the Incidence of Coughing During Emergence

Start date: January 2013
Phase: N/A
Study type: Interventional

This study is designed to compare the efficacy of endotracheal tube cuffs pre-filled with alkalinized lidocaine on the: - incidence of coughing during emergence of general anesthesia - time needed for emergence following a desflurane-based anesthesia - incidence of sore throat after extubation. The investigator's hypothesis is that the use of endotracheal tube cuffs pre-filled with alkalinized lidocaine will reduce the incidence of coughing by 50% relative to a control group following a desflurane-based anesthesia.

NCT ID: NCT01703923 Completed - Clinical trials for Chronic Refractory Cough

An Exploratory Study of FP01 Lozenges in Subjects With Chronic Refractory Cough

Start date: November 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the antitussive effect size and dose response of FP01 lozenges in subjects with chronic cough and to demonstrate the safety and tolerability of FP01 lozenges in subjects with chronic cough.

NCT ID: NCT01690975 Completed - Cough Clinical Trials

Benzonatate Dose Tolerance Study

Start date: July 2012
Phase: Phase 1
Study type: Interventional

This is a single-center, randomized, third party blind, placebo controlled, dose escalation study of benzonatate following single dose administration. The primary oobjective is to assess the safety and tolerability of increasing oral doses of benzonatate following single dose administration in healthy male and female subjects.