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NCT Number: NCT06833814

DOSE Trial: Optimal Dose of Oral Corticosteroids to Treat Asthma Exacerbations

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Treatment and study plan

Prednisone

Drug

Either 150 mg over 3 days or 250 mg over 7 days or 350 mg over 10 days

Primary outcomes

  1. Enrollment rate

    Time frame: 9 months

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

  2. Acceptability

    Time frame: 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.

Secondary outcomes

  1. Safety outcome: emergency room visits

    Time frame: 14 days

    Did the participant go to the emergency room visit between day of exacerbation and day 14.

  2. Safety outcomes: Hospitalization

    Time frame: 14 days

    Was the patient hospitalized between day of exacerbation and day 14?

  3. Safety outcomes: Unscheduled medical visits

    Time frame: 14 days

    Did the participant go for an unscheduled medical visit between day of exacerbation and day 14?

  4. Safety outcomes: increased or prolonged OCS dose

    Time frame: 14 days

    Has the participant had to increase or prolong his OCS dose?

  5. Safety outcomes: New or increase antibiotics

    Time frame: 14 days

    Was the participant prescribed new antibiotics treatment or had to increase antibiotics between day of exacerbation and day 14?

Other outcomes

  1. Success rate

    Time frame: 14 days

    Success parameters will include increased or prolonged OCS dose, re consultation for OCS, new, increased or prolonged antibiotics, change in ACQ6 score between baseline and 14 days, and change in FEV1 between baseline and 14 days.

Study contacts

Contact information is provided by the study sponsor or research team.

Andréanne Côté, MD-MSc

CONTACT

[email protected]

14186564747

Marie-Eve Boulay, MSc

CONTACT

[email protected]

418-656-8711

Sponsors and collaborators

Lead sponsor

Andréanne Côté

Other

Registry information

Official study title

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

Acronym: DOSE

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Feb 19, 2025
Registry last updated
Feb 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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