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临床试验/NCT04286464
NCT04286464Enrolling By Invitation不适用

Early Environmental and Maternal Determinants of Airway Inflammation in Wheezing Disorders in Infants

Insel Gruppe AG, University Hospital Bern1 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2003年9月最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
1,000
试验地点
1
主要终点
Change in Multiple Breath Washout

研究概览

简要总结

This study collects data on microbiological, genetic and environmental factors, as well as lung function parameters (e.g. spirometry, body plethysmography, lung-MRI) to assess the complex interaction of predisposing risk factors for impaired lung development and respiratory diseases.

详细描述

Background:

Lung development and growth is a complexly orchestrated process starting prenatally in the first embryonic weeks, and ending, with the last important stages of alveolarization from the 24th week onwards. By the time of birth, around one third of the total amount of alveoli has developed, while the rest develops during infancy and childhood. After birth, lung volume, airways and the gas-exchanging surface increase by a multiple, reaching the maximum lung size at around 25 years of age. A comprehensive understanding of lung growth and development is crucial in order to understand the pathophysiology of lung diseases. During childhood and ongoing lung growth, an important amount of respiratory diseases might develop.

Objectives:

Longitudinal assessment of lung growth and development, to examine respiratory morbidity such as Asthma and allergy, and the complex relationship between associated Risk factors mainly genetic predisposition and environmental factors on both lung development and subsequent respiratory morbidity, Therefore, longitudinal data on lung function and structure, on respiratory morbidity and on genetic, immunological, microbiological and environmental risk factors will be collected.

Methods:

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Term Born group (H): Healthy, white and term Born infants and Children. Born 38-42 weeks postconceptional.
  • Preterm group (P): Healthy, white preterm Born infants and Children. Born <37 weeks postconceptional. Which comply with the international criteria (Jobe and Bancalari) of a diagnosis of bronchopulmonary dysplasia (BPD), or of chronic lung disease of the new-born (CLD).
  • Risk pregnancy group (RP): White preterm Born infants and Children, including Twins. Born <37 weeks postconceptional. With fetal growth restriction (FGR), intrauterine growth restriction (IUGR) or preeclampsia (PE). With gestational Diabetes (GMD). With IVF or Amnion dysfunction.
  • Parents: language skills in German or French (by at least one parent).
  • Both of the parents can be Smokers and may be atopics (allergy of the mother and/or the Father).
  • Signed, written informed consent of the parents.

排除标准

  • Term Born group (H): Need of respiratory support > three days postnatal. Severe malformations or known diseases. Maternal drug abuse except smoking. Known sever maternal disease postpartum. Insufficient Knowledge of Project language (no German or French speaker). Pacemaker, continuous glucose monitor.
  • Preterm group (P): Severe malformations or known diseases. Maternal drug abuse except smoking. Known severe maternal disease postpartum. Insufficient Knowledge of Project language (no German or French speaker). Pacemaker, continuous glucose monitor.
  • Risk pregnancy group (RP): Insufficient Knowledge of Project language (no German or French speaker). Concurrent participation in another study. Participants, which lead to heterogeneity in genetic analysis and thus preclude any findings.

结局指标

主要结局

Change in Multiple Breath Washout

时间窗: Every third year from the age of 4-6 weeks/1 year till >16 years.

Longitudinal assessment of lung volume and ventilation inhomogeneity

Change in Spirometry

时间窗: Every third year from the age of 4-6 weeks/1 year till >16 years

Longitudinal assessment of long volumes

Change in Body plethysmography

时间窗: Every third year from the age of 4-6 weeks/1 year till >16 years.

Longitudinal assessment of ventilation inhomogeneity.

Change in Magnetic Resonance Imaging (MRI)

时间窗: At the age of 4-6 weeks, 1, 3, 6, 9, 12, 15 and >16 years.

Longitudinal assessment of regional lung perfusion and ventilation

Change in Nasal swabs

时间窗: At the age of 4-6 weeks, 1, 3, 6, 9, 12, 15 and >16 years.

Longitudinal assessment of viral and bacterial colonization of the nasal swab

Change in Weekly swabs

时间窗: Weekly from the visit at the age of 8-12 weeks till the age of 1 year.

Respiratory virus and bacterial diagnostic

Swabs during respiratory infection

时间窗: Any timepoint between the visit at the age of 4-6 weeks till the age of 1 year.

Respiratory viruses and Bacteria, changes of the microbial flora

次要结局

  • Environmental pollution markers(At the age of 4-6 weeks, 1, 3, 6, 9, 12, 15 and >16 years.)
  • Respiratory Rate (RR)(From the visit at the age of 4-6 weeks till the age of 1 year.)
  • Urine(At the age of 4-6 weeks.)
  • Cord blood(At birth.)
  • Capillary blood markers(At the age of 1, 3, 6, 9, 12, 15 and >16 years.)
  • Skin Prick Test(At the age of 3, 6, 9, 12, 15 and >16 years.)
  • Volatile organic compound markers(At the age of 4-6 weeks, 1, 3, 6, 9, 12, 15 and >16 years.)
  • Sputum(At the age of (3), 6, 9, 12, 15 and >16 years.)
  • Nasal brushes(At the age of 1, 3, 6, 9, 12, 15 and >16 years.)
  • Oropharyngeal swabs(At the age of 1, 3, 6, 9, 12, 15 and >16 years.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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