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Cough clinical trials

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NCT ID: NCT01659541 Completed - Clinical trials for Spinal Cord Injuries

Stimulation With Wire Leads to Restore Cough

Start date: April 2015
Phase: N/A
Study type: Interventional

The purpose of this trial is to determine the efficacy of spinal cord stimulation, using wire leads, to produce an effective cough in patients with spinal cord injuries.

NCT ID: NCT01659476 Completed - Asthma Clinical Trials

Bronchodilating and Bronchoprotective Effects of Deep Inspirations

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

The objectives of this research are to compare (i) the bronchodilating and (ii) the bronchoprotective effects of deep inspirations (DIs) in individuals with: (a) asthma, (b) CVA, (c) methacholine-induced cough but normal airway sensitivity and . (d) in healthy individuals (without asthma, chronic cough or asymptomatic airway hyperresponsiveness). Hypotheses: i. The bronchodilating effect of a DI will be: (a) absent or impaired in individuals with classic asthma; (b) impaired in individuals with CVA; (c) preserved in individuals with methacholine-induced cough but normal airway sensitivity; and (d) preserved in healthy individuals (without asthma, chronic cough or asymptomatic airway hyperresponsiveness). ii. The bronchoprotective effect of a DI will be: (a) absent in individuals with classic asthma; (b) impaired in individuals with CVA; (c) preserved in those with methacholine-induced cough but normal airway sensitivity; and (d) preserved in healthy individuals (without asthma, chronic cough or asymptomatic airway hyperresponsiveness). iii. Healthy individuals without asthma, chronic cough, or asymptomatic airway hyperresponsiveness, will not cough, or develop significant dyspnea, small airways obstruction or dynamic hyperinflation during high-dose methacholine bronchoprovocation.

NCT ID: NCT01656668 Completed - Cough Clinical Trials

Study of the Safety and Effectiveness of BC1036 Capsules to Treat Frequent Long-Term Cough

Start date: July 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the effect of BC1036 (theobromine) on cough-related quality of life and cough severity following 2 weeks' treatment.

NCT ID: NCT01637649 Completed - Cough Clinical Trials

Diaphragmatic Function in Stroke Patients.

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

- This study attempts to elucidate whether stroke patients with dysphagia have reduced diaphragm movement during voluntary coughing, and also during deep inspiration and expiration than stroke patients without dysphagia. - This study will also compare various spirometric measurements with the diaphragmatic motions.

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: NCT01597349 Completed - Acute Cough Clinical Trials

Antitussive Effects of FP01 Lozenges in Subjects With Cough Due to Upper Respiratory Tract Infection

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

The purpose of this research study is to learn how effective and safe FP01 lozenges are when given to subjects with a cough due to an upper respiratory tract infection. The study will include subjects who have an upper respiratory tract infection, with a cough of less than six weeks duration.

NCT ID: NCT01588249 Terminated - Cough Clinical Trials

A Novel Formulation of Pasteurized Maple Cough Syrup Compared With Placebo on Nocturnal Cough and Sleep Quality in Infants With Upper Respiratory Infection

Start date: April 2012
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. A product that has been used in alternative medicine for cough is maple syrup. Although no studies have formally evaluated the use of maple syrup for nocturnal cough associated with URI, the demulcent effect of maple syrup may provide some relief from cough in children. A novel formulation of pasteurized maple cough syrup, when compared to placebo, should provide superior relief on nocturnal cough and the sleep difficulty associated with URI in children under 12 months and sleep difficulty of their parent/caregiver.

NCT ID: NCT01587716 Completed - Cough Clinical Trials

A Study to Investigate the Safety, Tolerability and Pharmacokinetics of GSK2339345.

Start date: April 23, 2012
Phase: Phase 1
Study type: Interventional

This is a study of the sodium channel inhibitor, GSK2339345. Cohort 1 will assess the safety, tolerability and PK of single ascending doses of GSK2339345 administered via an aqueous droplet inhaler in healthy subjects. Cohort 2 will assess the safety, tolerability, and PK of repeat doses of GSK2339345 administered four times a day for two consecutive days via an aqueous droplet inhaler.

NCT ID: NCT01575821 Completed - Sleep Clinical Trials

The Effect of Honey on Nocturnal Cough and Sleep Quality

Start date: January 2009
Phase: N/A
Study type: Interventional

Cough is a common symptom in pediatric practice. It can be particularly troubling to children and their parents.It often results in discomfort to the child and loss of sleep to both the child and the parent. The objective of this trial was to compare the effects on nocturnal cough and the sleep difficulty associated with URIs of a single nocturnal dose of three different honey products compared to placebo

NCT ID: NCT01566968 Completed - Healthy Clinical Trials

Novel Endpoints in Cough Challenge Testing

NEAT
Start date: January 2011
Phase: N/A
Study type: Observational

The sensitivity of a person's cough reflex can be measured by getting them to breathe in (inhale) irritant chemicals. There are different methods by which subjects are asked to inhale these chemicals, either by taking one deep breath in, or by asking them to just continue to take a number of breaths. The purpose of this clinical research study is to see if the coughing responses are different in healthy people and people with respiratory problems that make them cough when they are given these chemicals in these two methods.