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临床试验/NCT05795712
NCT05795712已完成不适用

'Real Life' Monitoring of COPD Patients According to the 2017 GOLD Recommendations: Role of Bronchial Inflammation in Patient Management.

Istituti Clinici Scientifici Maugeri SpA1 个研究点 分布在 1 个国家目标入组 53 人开始时间: 2017年6月28日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
53
试验地点
1
主要终点
Number of participants which introduced ICS therapy after 24 month of follow up

研究概览

简要总结

The aim of the study will be to assess in patients with mild-to-moderate COPD the role of inflammation in the patient's therapeutic management and follow-up.

详细描述

Studies have already shown that the risk of severe exacerbations in patients with COPD is associated with eosinophilic inflammation (1) and that patients with this type of inflammation have an increased risk of exacerbations if ICS administration is discontinued (2), but this indication does not appear in the latest GOLD recommendations to date.

The aim of the study will be to evaluate in patients with mild-to-moderate COPD the role of induced sputum and peripheral inflammation in the patient's therapeutic management and follow-up. For this purpose, the investigators will assess inflammation at the bronchial and systemic level by induced sputum and haemochrome at time 0 (recruitment), after 6,12, 18 and 24 months after therapy administration according to the updated 2017 GOLD recommendations.

研究设计

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

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • COPD diagnosis according to GOLD 2017 recommendations in clinical stability phase
  • Post bronchodilator FEV1 ≥50 and ≤80
  • Both smoker and ex-smoker
  • Patients on LABA or LABA/LAMA therapy
  • Patients also on ICS therapy discontinued at least 30 days after enrolment
  • Patient able to cooperate with the required procedures
  • Patient who has signed the informed consent

排除标准

  • - Acute respiratory episode treated with antibiotics and/or steroids in the lower 4 weeks prior to enrolment
  • Patients on roflumilast therapy
  • Any exacerbation of COPD within 1 month after visit
  • A patient must not have had any hospitalisation for COPD within 6 months prior to visit
  • Comorbidities. History or current evidence of a clinically significant comorbidity or history of a positive test for HIV, hepatitis B or hepatitis C.
  • History of adverse reactions including immediate or delayed hypersensitivity to any beta2-agonists,
  • sympathomimetic drugs or any intranasal, inhaled or systemic corticosteroid therapy known or suspected sensitivity to the components of the inhalers used in the study (e.g. lactose in dry powder inhalers).
  • Use of immunosuppressive drugs within 12 weeks prior to visit 1 and during the study, including use of systemic corticosteroids.

结局指标

主要结局

Number of participants which introduced ICS therapy after 24 month of follow up

时间窗: 24 months

The aim of our study will be to evaluate in patients with mild-to-moderate COPD the role of inflammation in the patient's therapeutic management and follow-up.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

RicercaTradate

Professor Antonio Spanevello

Istituti Clinici Scientifici Maugeri SpA

研究点 (1)

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