NCT00413140已完成不适用
Biomarkers in Exhaled Breath Indicate Presence, Control and Severity of Cystic Fibrosis
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 100
- 试验地点
- 4
研究概览
简要总结
Background Chronic airway inflammation is present in cystic fibrosis. Non-invasive inflammometry may be useful in disease management.
Objective We studied 1) the ability of fractional exhaled nitric oxide and inflammatory markers (acidity, nitrite, nitrate, hydrogen peroxide, 8-isoprostane, interferon-γ, tumor necrosis factor-α, interleukin-2,-4,-5,-10) in exhaled breath condensate, to discriminate between cystic fibrosis and control children, and, 2) the relationship of biomarkers with control and severity of cystic fibrosis.
Methods In 98 children (48 cystic fibrosis / 50 controls), condensate was collected using a glass condenser. Exhaled nitric oxide was measured using the NIOX®.
研究设计
- 研究类型
- Observational
- 时间视角
- Other
入排标准
- 年龄范围
- 5 Years 至 25 Years(Child, Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •CF population
- •Children known with CF were recruited from the outpatient clinics. CF disease was defined as a combination of typical clinical features (e.g. persistent pulmonary problems, meconium ileus, failure to thrive, steatorrhoe) and an abnormal sweat test (Chloride > 60 mM). Uncontrolled CF was diagnosed by the paediatric pulmonologist based on a change in the presence or severity of respiratory symptoms in association with CF, and/or a decrease in lung function parameters compared to previous measurements during the last four weeks.
- •Control population
- •Control children without lung disease were recruited from the outpatient clinic of the University Hospital Maastricht. The reasons of consultation were constipation and enuresis nocturna. All children completed the 'International Study of Asthma and Allergies in Childhood (ISAAC) questionnaire to exclude children with any (history of) airway or allergy complaints, in order to exclude asthmatic disease
排除标准
- •For both study populations:
- •Diseases that may interfere with the results of the study (e.g. upper airway infection, heart disease, anatomic abnormalities of the airways and other chronic inflammatory diseases, such as Crohns disease and rheumatoid arthritis)
- •Mental retardation
- •Inability to perform the EBC collection procedure
- •Active smoking
- •Use of the following medication: papaverin, sodium nitroprusside, angiotensin-converting enzyme (ACE) inhibitors, oxymetazoline, L-arginine, or nitric oxide synthase (NOS) inhibitors.
研究者
研究点 (4)
Loading locations...
相似试验
已完成
不适用
Assessment of Cystic Fibrosis Lung Involvement With UTE Pulse SequencesCystic FibrosisNCT02449785University Hospital, Bordeaux30
已完成
不适用
A Novel Assay to Quantify Treatment Response in Cystic Fibrosis (CF)Cystic FibrosisNCT01626157Milene Saavedra122
已完成
3 期
Study to Evaluate Arikayce™ in CF Patients With Chronic Pseudomonas Aeruginosa InfectionsPseudomonas Aeruginosa InfectionNCT01315678Insmed Incorporated302
已完成
不适用
Functional Analysis by Dynamic Imaging of the Respiratory Epithelium in Infants With Cystic FibrosisCystic FibrosisNCT01605565Institut National de la Santé Et de la Recherche Médicale, France30
撤回
3 期
Study to Evaluate Arikace™ in CF Patients With Chronic Infection Due to Pseudomonas AeruginosaCystic FibrosisNCT01315691Insmed Incorporated
