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Streamlined Treatment of Pulmonary Exacerbations in Pediatrics

Recruiting

Streamlined Treatment of Pulmonary Exacerbations in Pediatrics Randomized Controlled Trial (STOP PEDS RCT)

Who can join

Ages 3 to 18 · All sexes

Full eligibility criteria
Inclusion Criteria:

1. Age

   1. For main cohort and non-HEMT cohort: age 6 to \<19 years
   2. For preschool cohort: age 3 to \<6 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. Highly Effective Modulator Therapy

   1. For main cohort and preschool cohort: Taking HEMT for at least 3 months at enrollment
   2. For non-HEMT cohort: not eligible for HEMT based on CFTR genotype or eligible but not taking for at least 3 months and no plans to start HEMT in the next year, and also not taking tezacaftor-ivacaftor or lumacaftor-ivacaftor for at least 3 months
5. For main cohort and non-HEMT cohort: able to perform acceptable and reproducible spirometry
6. For main cohort and non-HEMT cohort: ppFEV1 ≥ 50% predicted at enrollment based on the Global lung Initiative (GLI) reference equations
7. Ability to receive text messages and access the internet

Exclusion Criteria:

1. Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the individual or the quality of the data
2. Receiving an acute course of oral or IV antibiotics at the time of enrollment or within the 14 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
3. Treatment with systemic corticosteroids at enrollment or within the 14 days prior to enrollment. Individuals may be re- screened ≥21 days after completion of systemic corticosteroids if they are at their clinical baseline, per self-report
4. History of solid organ transplant
5. History of positive culture for Mycobacterium abscessus in the 12 months prior to enrollment
6. Treatment with antibiotics for any non-tuberculous mycobacteria (NTM) at enrollment
7. Three or more IV antibiotic-treated PEx in the 12 months prior to enrollment
8. Treatment with chronic oral antibiotics other than azithromycin at enrollment
9. Treatment with systemic corticosteroids for allergic bronchopulmonary aspergillosis (ABPA) in the 12 months prior to enrollment

About the study

The STOP PEDS RCT is a multicenter, parallel, open label randomized controlled trial evaluating the long-term (one year) and short-term safety and efficacy of two antibiotic treatment strategies for the management of outpatient pulmonary exacerbations (PEx) in the pediatric CF population.

What is being tested

Sponsor: University of Washington, the Collaborative Health Studies Coordinating Center · Participants: 430 · Started: Dec 1, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT06654752

Locations in the U.S.

AlabamaThe Children's Hospital Alabama & University of Alabama at Birmingham, Birmingham
ArizonaTucson Cystic Fibrosis Center, Tucson
CaliforniaChildren's Hospital of Los Angeles & Anton Yelchin Cystic Fibrosis Clinic, Los Angeles
Stanford University, Palo Alto
Rady Children's Hospital at University of California San Diego, San Diego (Not yet recruiting)
ColoradoChildren's Hospital of Colorado, Aurora
GeorgiaChildren's Healthcare of Atlanta & Emory University, Atlanta
IllinoisAnn & Robert H. Lurie Children's Hospital of Chicago & Northwestern University, Chicago
IndianaRiley Hospital for Children & Indiana University, Indianapolis
IowaUniversity of Iowa, Iowa City
MarylandJohns Hopkins Hospital, Johns Hopkins University, Baltimore
MassachusettsBoston Children's Hospital & Harvard University, Boston
MichiganUniversity of Michigan Health System, Ann Arbor
MinnesotaChildren's Hospitals and Clinics of Minnesota, Minneapolis
The Minnesota Cystic Fibrosis Center & University of Minnesota, Minneapolis
MissouriChildren's Mercy Hospital, Kansas City
St. Louis Children's Hospital & Washington University School of Medicine, St Louis
New YorkUniversity of Rochester Medical Center Strong Memorial, Rochester
North CarolinaUniversity of North Carolina at Chapel Hill, Chapel Hill
OhioCincinnati Children's Hospital Medical Center, Cincinnati
OregonOregon Health & Science University, Portland
PennsylvaniaChildren's Hospital of Philadelphia & University of Pennsylvania, Philadelphia
Children's Hospital of Pittsburgh of UPMC & University of Pittsburgh Medical Center, Pittsburgh
South CarolinaMedical University of South Carolina, Charleston
TexasUniversity of Texas Southwestern & Children's Health, Dallas
Texas Children's Hospital & Baylor College of Medicine, Houston
VermontVermont Children's Hospital & University of Vermont Medical Center, Burlington
VirginiaVirginia Commonwealth University, Richmond
WashingtonSeattle Children's Hospital, Seattle
WisconsinUniversity of Wisconsin, Madison
Children's Wisconsin & Medical College of Wisconsin, Milwaukee

Conditions

From ClinicalTrials.gov, data retrieved Oct 3, 2026. Each study sets its own eligibility; the study team decides who can join.