Cystic Fibrosis
Conditions
Keywords
cystic fibrosis, oral antibiotics, pulmonary exacerbation, pediatric
Brief summary
STOP PEDS is a pilot study of children with CF ages 6-18 across 10 sites in North America. The primary goal is to assess the acceptability and feasibility of a multicenter randomized trial comparing immediate antibiotics versus tailored therapy for pulmonary exacerbation (PEx) treatment in this population.
Detailed description
STOP PEDS is a pilot study of children with CF ages 6-18 across 10 sites in North America. The primary goal is to assess the acceptability and feasibility of a multicenter randomized trial comparing immediate antibiotics versus tailored therapy for pulmonary exacerbation (PEx) treatment in this population. The primary endpoint is the proportion of participants in the tailored arm who did not take any oral antibiotics in the 28 days following randomization. Ultimately, we want to learn: * What is the best way to treat pulmonary exacerbations? * Should everyone with a pulmonary exacerbation take antibiotics? * Do the benefits of starting antibiotics at the first signs of illness outweigh the possible risks, like side effects and antibiotic resistance? This pilot study is designed to determine if an interventional study to help answer these questions is feasible. Up to 120 participants will be enrolled and followed through their well state of health, then for 28 days following their first randomized exacerbation. Enrollment will stop after 80 pulmonary exacerbation events have been randomized, even if this does not require 120 participants. Due to the nature of the study, the identity of treatment assignment will be known to investigators, research staff, and patients (ie, not blinded). Total duration of this pilot study is expected to be approximately 18 months: 6 months for participant recruitment and 12 months for follow up. Participants could be monitored for up to 18 months if they do not have an exacerbation. However, it is anticipated that the majority of participants will experience a randomizable PEx event and therefore have a shorter follow up period.
Interventions
OTHERImmediate Antibiotics
increase airway clearance/start oral antibiotics right away
OTHERTailored Treatment
increase airway clearance and start oral antibiotics later if symptoms get worse or do not get better
Sponsors
Cystic Fibrosis Foundation
University of Washington, the Collaborative Health Studies Coordinating Center
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
6 Years to 18 Years
Healthy volunteers
No
Inclusion criteria
Enrollment Inclusion Criteria: 1. Age 6 to \<19 years 2. Documentation of a CF diagnosis as evidenced by one or more clinical features consistent with the CF phenotype and one or more of the following criteria: 1. sweat chloride ≥ 60 mEq/liter 2. two disease-causing variants in the cystic fibrosis transmembrane conductive regulator (CFTR) gene 3. Written informed consent (and assent when applicable) obtained from participant or participant's legal representative and ability of participant to comply with the requirements of the study 4. Able to perform acceptable and reproducible spirometry 5. FEV1 ≥ 50% predicted at enrollment based on the Global lung Initiative (GLI) reference equations 6. At least 1 course of oral or IV antibiotics for respiratory symptoms since January 1, 2019. 7. Ability to receive text messages and access the internet Enrollment
Exclusion criteria
1. Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data. 2. Previous randomization in the study 3. Receiving antibiotics for a PEx at the time of enrollment or within the 21 days prior to enrollment. Individuals may be re-screened ≥21 days after completion of antibiotics if they are at their baseline state of health, per self-report. 4. Treatment with systemic corticosteroids at enrollment. Individuals may be re- screened ≥21 days after completion of systemic corticosteroids if they are at their clinical baseline, per self-report. 5. History of solid organ transplant 6. History of positive culture for Mycobacterium abscessus in the 12 months prior to enrollment 7. Treatment with antibiotics for any non-tuberculous mycobacteria (NTM) at enrollment 8. Three or more IV antibiotic-treated PEx in the 12 months prior to enrollment 9. Treatment with chronic oral antibiotics other than azithromycin at enrollment
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Delayed antibiotics | 28 days | The proportion of participants in the tailored arm who did not take any oral antibiotics in the 28 days following randomization |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pulmonary Exacerbations Reported | 18 months | Proportion of Pulmonary Exacerbations in which symptoms are reported within 7 days of onset |
| Randomization Criteria | 18 months | Proportion of Pulmonary Exacerbation events meeting randomization criteria |
| Consent | 6 months | Proportion of approached patients consenting to enroll |
| Randomized Exacerbations | 18 months | Proportion of randomizable Pulmonary Exacerbations that undergo randomization |
| Day 28 Follow-up | 18 months | Proportion of participants with a randomized Pulmonary Exacerbation that attends an in-person Day 28 follow up visit |
| Participant Exacerbations | 18 months | Proportion of enrolled participants experiencing a randomizable Pulmonary Exacerbation |
Countries
United States
Outcome results
None listed