このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

Characterization of Adults for Asthma Microbiome Research Studies (CAARS)

2022年7月18日 更新者: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.

調査の概要

状態

完了

条件

詳細な説明

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.

研究の種類

観察的

入学 (実際)

171

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Michigan
      • Ann Arbor、Michigan、アメリカ、48109
        • University of Michigan

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~75年 (大人、高齢者)

健康ボランティアの受け入れ

はい

受講資格のある性別

全て

サンプリング方法

確率サンプル

調査対象母集団

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

説明

  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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

コホートと介入

グループ/コホート
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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
時間枠
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
時間枠:Day 1" for the first one and "up to 60 days"
Day 1" for the first one and "up to 60 days"

二次結果の測定

結果測定
時間枠
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
時間枠:Day 1" for the first one and "up to 60 days"
Day 1" for the first one and "up to 60 days"

その他の成果指標

結果測定
時間枠
To apply culture and molecular methods to study functions of asthma-associated airway microbiota in corticosteroid-enriched environments
時間枠: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
時間枠: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
時間枠:Day 1" for the first one and "up to 60 days"
Day 1" for the first one and "up to 60 days"

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Yvonne J. Huang, MD、University of Michigan

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2015年12月22日

一次修了 (実際)

2020年3月13日

研究の完了 (実際)

2020年3月13日

試験登録日

最初に提出

2016年8月29日

QC基準を満たした最初の提出物

2016年8月29日

最初の投稿 (見積もり)

2016年9月2日

学習記録の更新

投稿された最後の更新 (実際)

2022年7月20日

QC基準を満たした最後の更新が送信されました

2022年7月18日

最終確認日

2022年7月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • HUM00097163
  • 5R01AI129958 (米国 NIH グラント/契約)

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

3
購読する