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Characterization of Adults for Asthma Microbiome Research Studies (CAARS)

18 juillet 2022 mis à jour par: Yvonne J Huang, University of Michigan

Characterization of Adults for Asthma Microbiome Research Studies (CAARS)

The purpose of this study is to characterize adult subjects regarding their history of allergy and asthma, clinical manifestations of asthma, and exposures and conditions that may influence asthma severity and control. Assessments include baseline medical history, lung function tests, questionnaires, and collection of specimens for phenotypic characterization.

Aperçu de l'étude

Statut

Complété

Les conditions

Description détaillée

This is a prospective, observational study in which approximately 200 subjects will be enrolled, including healthy controls, atopic controls without asthma, and patients with stable asthma (n = 150). Among asthmatics, 2/3 will be on regular inhaled corticosteroid therapy and 1/3 will not be taking inhaled corticosteroids. Subjects who meet study criteria will undergo phenotypic characterization in multiple domains, including evaluation of lung function, assessments of asthma/allergy history, asthma triggers, asthma symptom control, environmental microbial exposures and dietary intake. Oral rinse, sputum, stool, urine and blood specimens will be collected for microbiome-related analyses, including molecular and culture-based assays, metabolite studies, and to relate these to markers of inflammation and immune function. The overall goal is to enroll a cohort of well-characterized asthmatic and non-asthmatic control subjects to enable mechanism-oriented studies of how members of the airway microbiota and possibly also gut microbiota influence phenotypes of adult asthma.

Type d'étude

Observationnel

Inscription (Réel)

171

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Michigan
      • Ann Arbor, Michigan, États-Unis, 48109
        • University of Michigan

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 75 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

Méthode d'échantillonnage

Échantillon de probabilité

Population étudiée

A cohort of well characterized asthmatic subjects and a cohort of healthy people without asthma.

La description

  1. For all subjects:

    Inclusion criteria:

    - Men/Women, ages 18-75, with or without current asthma, are eligible to be screened.

    Exclusion criteria:

    • Cigarette smoking history of >30 total pack-years
    • Current use of other smoked products or recreational drugs (e.g. pipes, cigars, e-cigarettes, other illicit drugs)
    • History of lung disease other than asthma
    • Recent upper respiratory tract infection treated with antibiotics within 8 weeks of visit 1
    • Recent antibiotic use (except topical or ocular) within 8 weeks of visit 1 (chronic antibiotic use for asthma management allowed)
    • Currently pregnant or breast-feeding
    • Other medical conditions or treatments that may increase subject risk or affect study results, based on study physician judgment. These include the following: significant cardiovascular disease(+/- active symptoms), arrhythmia, or stroke, active cancer, post-organ transplant
    • Any other condition for which subject is taking immunosuppressive therapies (except steroids for asthma)
    • History of allergy to albuterol or methacholine
  2. For asthma subjects only:

    Note: Enrollment target is for 90 asthmatics already taking inhaled corticosteroids prescribed by their physician (any formulation and dose) and 60 subjects who are not currently using inhaled corticosteroid.

    Additional inclusion criteria:

    • History of asthma symptoms within the last 2 years (e.g. wheeze, shortness of breath, etc.)
    • Evidence of stable asthma as assessed by initial screening
    • No changes in asthma medications within 30 days of visit 1
    • Methacholine PC20 (dose at which there is a 20 percent change) ≤ 8 mg/ml (for those asthmatics on inhaled steroids, PC20 ≤ 16 mg/ml), or change in FEV1 (forced expiratory volume in first second of spirometry effort)≥ 12% after 4 puffs of albuterol on reversibility testing (or PI discretion)
    • If negative methacholine challenge or no evidence of bronchodilator reversibility, a strong history of physician-diagnosed/physician-managed asthma may allow for study inclusion, based on PI's judgement or discretion.
    • Individuals with a history of physician-diagnosed asthma who have had bronchodilator reversibility testing or methacholine challenge performed within 60 days of screening may be enrolled and these existing test results used in lieu of repeating the same test at visit 1 or visit 2.

    Additional exclusion criteria:

    • An asthma exacerbation requiring treatment with oral or IV steroids within 1 month of visit 1
    • No asthma symptoms within the last 2 years
  3. For healthy control or atopic non-asthma subjects:

Additional exclusion criteria:

  • Evidence of abnormal lung function by any of the following: FEV1/FVC ratio <0.70, FEV1 or FVC (forced vital capacity on spirometry) < 80% predicted, methacholine PC20 < 16 mg/ml, or FEV1 improvement > 12% in response to albuterol
  • Atopic non-asthma subjects found to have evidence of abnormal lung function, but without a clear or recent history of asthma, may be enrolled per PI's discretion.
  • Possible pulmonary disease is identified by PI or Co-Is to explain an abnormal lung function result at the time of testing. The subject may be re-screened later at investigator's discretion.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

Cohortes et interventions

Groupe / Cohorte
Asthmatic, not taking inhaled steroids
Men/Women, ages 18-75 who are not currently taking corticosteroids.. No intervention; this is a prospective observational study.
Asthmatic, taking inhaled steroids
Men/Women, ages 18-75 who are already taking corticosteroids prescribed by their physician. No intervention; this is a prospective observational study.
Healthy, non-asthmatic without allergies
Men/Women, ages 18-75 without a current diagnosis of asthma and no allergies. No intervention; this is a prospective observational study.
Healthy, atopic non-asthmatic
Men/Women, ages 18-75 with allergies but without a current diagnosis of asthma. No intervention; this is a prospective observational study.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
To characterize adult subjects with asthma in multiple domains, including disease severity and control, patterns of airway inflammation, microbial exposures and patterns of airway and gut microbial colonization
Délai: Day 1" for the first one and "up to 60 days"
Day 1" for the first one and "up to 60 days"

Mesures de résultats secondaires

Mesure des résultats
Délai
To evaluate differences in airway and gut microbiota composition related to inhaled corticosteroid use (ICS) among asthmatics already regularly taking ICS, asthmatics not taking ICS, and healthy controls
Délai: Day 1" for the first one and "up to 60 days"
Day 1" for the first one and "up to 60 days"

Autres mesures de résultats

Mesure des résultats
Délai
To apply culture and molecular methods to study functions of asthma-associated airway microbiota in corticosteroid-enriched environments
Délai: Day 1" for the first one and "up to 60 days"
Day 1" for the first one and "up to 60 days"
To evaluate the temporal stability of the airway microbiome in asthmatic and healthy subjects
Délai: Day 1" for the first one and "up to 60 days"
Day 1" for the first one and "up to 60 days"
To explore relationships between airway and gut microbiome composition in asthma, including among obese subjects
Délai: Day 1" for the first one and "up to 60 days"
Day 1" for the first one and "up to 60 days"

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Yvonne J. Huang, MD, University of Michigan

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

22 décembre 2015

Achèvement primaire (Réel)

13 mars 2020

Achèvement de l'étude (Réel)

13 mars 2020

Dates d'inscription aux études

Première soumission

29 août 2016

Première soumission répondant aux critères de contrôle qualité

29 août 2016

Première publication (Estimation)

2 septembre 2016

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

20 juillet 2022

Dernière mise à jour soumise répondant aux critères de contrôle qualité

18 juillet 2022

Dernière vérification

1 juillet 2022

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • HUM00097163
  • 5R01AI129958 (Subvention/contrat des NIH des États-Unis)

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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