Exhaled Breath Condensate Biomarkers and Cough in IPF

Exhaled Breath Condensate Biomarkers and Cough in People With Idiopathic Pulmonary Fibrosis

Patrocinadores

Patrocinador principal: University of East Anglia

Fuente University of East Anglia
Resumen breve

Analysis of exhaled breath condensate biomarkers and cough severity in patients with idiopathic pulmonary fibrosis.

Descripción detallada

This study will aim to investigate the levels of the reactive oxygen species (ROS) 8-isoprostane in idiopathic pulmonary fibrosis patients' exhaled breath condensate (EBC). EBC samples will be collected using RTube, prior to analysis for levels of 8-isoprostane. An acceptability assessment will be performed for this non-invasive method of EBC collection through a non-validated questionnaire.

A regression analysis will then be performed for 8-isoprostane levels against the severity of the patient's cough, assessed through the use of the visual analogue scale for cough (VAS), the King's brief interstitial lung disease questionnaire (KBILD), the Medical Research Council (MRC) dyspnoea scale and the Leicester cough questionnaire. Alongside this an exploratory comparison of cough scores and 8 isoprostane concentration between patients with and without honeycombing and traction bronchiectasis.

Estado general Completed
Fecha de inicio January 2016
Fecha de Terminación June 2016
Fecha de finalización primaria June 2016
Tipo de estudio Observational
Resultado primario
Medida Periodo de tiempo
8-isoprostane levels 1 day (Single measurement )
Resultado secundario
Medida Periodo de tiempo
Leicester Cough Questionnaire 1 day (Single measurement )
Kings brief interstitial lung disease questionnaire 1 day (Single measurement )
MRC dyspnoea Scale 1 day (Single measurement )
Visual analogue scale for Cough 1 day (Single measurement )
Non-validated acceptability questionnaire 1 day (Single measurement )
Inscripción 52
Condición
Elegibilidad

Método de muestreo: Non-Probability Sample

Criterios:

Inclusion Criteria:

- Male or female above the age of 40

- IPF diagnosed by a multi-disciplinary team meeting following review of clinical history, thoracic high resolution computed tomography (HRCT) and/or surgical lung according to international guidelines

Exclusion Criteria:

- A recognised significant co-existing respiratory disease, defined as a respiratory condition that exhibits a clinically relevant effect on respiratory symptoms and disease progression as determined by the principal investigator following multi-disciplinary discussion. For example, patients with bronchiectasis will only be included if the bronchiectasis is deemed to be traction bronchiectasis as a result of idiopathic pulmonary fibrosis

- Airflow obstruction defined as a forced expiratory volume at one second over forced vital capacity (FEV1/FVC) <60% predicted or a residual volume greater than 120% predicted

- Significant medical ,surgical or psychiatric disease that in the opinion of the patient's attending physician would exhibit a clinically relevant effect on the patient's health related quality of life

- The patient is unable to provide written informed consent

Género: All

Edad mínima: 40 Years

Edad máxima: N/A

Voluntarios Saludables: No

Oficial general
Ubicación
Instalaciones: University of East Anglia
Ubicacion Paises

United Kingdom

Fecha de verificación

June 2016

Fiesta responsable

Tipo: Sponsor

Tiene acceso ampliado No
Condición Examinar
Grupo de brazo

Etiqueta: Idiopathic pulmonary fibrosis sufferers

Descripción: Male or female idiopathic pulmonary fibrosis (IPF) sufferers over the age of 40, with a confirmed diagnosis of IPF against international guidelines. Patients are devoid of significant other medical, surgical or psychiatric illnesses that may affect respiratory symptoms or disease progression.

Información de diseño del estudio

Modelo de observación: Cohort

Perspectiva de tiempo: Cross-Sectional

Fuente: ClinicalTrials.gov