Prednisone
DrugEither 150 mg over 3 days or 250 mg over 7 days or 350 mg over 10 days
NCT Number: NCT06833814
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.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Phase 4
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Either 150 mg over 3 days or 250 mg over 7 days or 350 mg over 10 days
Time frame: 9 months
Period of time needed to recruit the total number of subjects.
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.
Time frame: 14 days
Did the participant go to the emergency room visit between day of exacerbation and day 14.
Time frame: 14 days
Was the patient hospitalized between day of exacerbation and day 14?
Time frame: 14 days
Did the participant go for an unscheduled medical visit between day of exacerbation and day 14?
Time frame: 14 days
Has the participant had to increase or prolong his OCS dose?
Time frame: 14 days
Was the participant prescribed new antibiotics treatment or had to increase antibiotics between day of exacerbation and day 14?
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.
Contact information is provided by the study sponsor or research team.
Andréanne Côté, MD-MSc
CONTACT
Marie-Eve Boulay, MSc
CONTACT
Andréanne Côté
Other
DOSE Trial: Optimal Dose of Oral Corticosteroids to Treat Asthma Exacerbations: A Parallel, Randomized Controlled Pilot Study
Acronym: DOSE
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.
Published trials that share one or more normalized conditions with this study.
NCT07396987
Asthma, Asthma Attack
View Trial DetailsNCT07112456
Asthma, Asthma Acute
View Trial DetailsNCT06750354
Anaemia, Anemia
View Trial DetailsNCT07731217
Asthma, Asthma (Diagnosis)
Istanbul, Turkey (Türkiye)
View Trial Details