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临床试验/NCT06833814
NCT06833814尚未招募4 期

DOSE Trial: Optimal Dose of Oral Corticosteroids to Treat Asthma Exacerbations: A Parallel, Randomized Controlled Pilot Study

Andréanne Côté0 个研究点目标入组 36 人开始时间: 2025年2月17日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
36
主要终点
Enrollment rate

研究概览

简要总结

Patients with severe asthma frequently experience exacerbations of their disease. The heterogeneity of asthma exacerbations represents a major challenge for patients and healthcare providers, making treatment difficult. Current guidelines recommend varying doses of short-term oral corticosteroids (OCS) as first-line treatment for asthma exacerbations. However, studies supporting the optimal dose of OCS to treat asthma exacerbations are rare.

This study aims to evaluate the feasibility, acceptability, and safety of a randomized clinical trial with different OCS regimens for patients and physicians. Additionally, evaluate the success rate of different OCS dosages to support power calculations for a non-inferiority trial.

In this pilot, parallel, randomized, controlled study, patients with severe asthma exacerbation, considered to require treatment with OCS according to physician judgment after a complete evaluation will be randomized to 1) 3 days of 50 mg prednisone followed by 7 days of placebo, 2) 3 days of 50 mg prednisone and 4 days of 25 mg prednisone followed by 3 days of placebo, or 3) 5 days of 50 mg prednisone and 5 days of 25 mg prednisone. Randomized patients will be assessed for daily symptoms and overall perception of well-being, in addition to asthma control, quality of life as well as additional medical visits. Lung function and inflammation will also be measured. Feasibility and acceptability will be defined by a participation rate >80%, while safety will be defined as an increase in OCS doses in <20% of patients in one arm or an emergency room visit in <10% of patients in one arm. Success will be defined as no increased or prolonged doses of OCS, no re-consultation for OCS or escalation to antibiotics, reduction of symptoms, and return of lung function to >80% of its optimal level.

In addition to determining the feasibility and safety of different OCS regimens to treat asthma exacerbations, this trial will help us determine the optimal design for a randomized clinical trial using different OCS regimens. The exacerbation clinic is already operational with 4 to 5 patients/week assessed and treated. We have all the resources on site to carry out this project.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • •Male and female volunteers
  • •18 years of age or older
  • •Assessed for a severe asthma exacerbation
  • •Being prescribed OCS for the management of their exacerbation
  • •Able to comprehend and follow all required study procedures
  • •Able to understand and give written informed consent and have signed a written informed consent form (ICF) approved by the REB

排除标准

  • •For females, are pregnant, or lactating
  • •Respiratory comorbidities other than asthma, including bronchiectasis (non-CF) or asthma-COPD overlap (ACO)
  • •FEV1 <40% of personal best or <1 Li
  • •OCS-dependent
  • •Asthma exacerbation in the 4 weeks preceding the study visit
  • •Concomitant disease, health condition, and/or lifestyle activities that could interfere with the conduct of the study, or for which the treatment might interfere with the conduct of the study, or that would, in the opinion of the Investigator, pose an unacceptable risk to the participant in this study, including, but not limited to, cancer, alcoholism, drug dependency or abuse, or psychiatric disease. These include, but are not restricted to: heart failure, previous bipolar decompensation with prednisone, severe blood hypertension, uncontrolled diabetes, pneumonia.
  • •Unwilling or unable to comply with the study protocol for any other reason

研究组 & 干预措施

Small-dose short-course

Experimental

3 days of 50 mg of prednisone followed by 7 days of placebo

干预措施: Prednisone (Drug)

High-dose long-course

Active Comparator

5 days of 50 mg of prednisone and 5 days of 25 mg of prednisone

干预措施: Prednisone (Drug)

Usual care

Active Comparator

3 days of 50 mg of prednisone and 4 days of 25 mg of prednisone followed by 3 days of placebo

干预措施: Prednisone (Drug)

结局指标

主要结局

Enrollment rate

时间窗: 9 months

Period of time needed to recruit the total number of subjects.

Acceptability

时间窗: 9 months

Acceptability for subjects will be defined by the proportion of subjects agreeing to the study whereas acceptability for physicians will be defined by the proportion of subjects for whom the physicians prescribe OCS and is willing to enroll them in the study.

次要结局

  • Safety outcome: emergency room visits(14 days)
  • Safety outcomes: Hospitalization(14 days)
  • Safety outcomes: Unscheduled medical visits(14 days)
  • Safety outcomes: increased or prolonged OCS dose(14 days)
  • Safety outcomes: New or increase antibiotics(14 days)

研究者

发起方
Andréanne Côté
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Andréanne Côté

Respirologist-intensivist

Laval University

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