Administering NMT to Reestablish Infant Nasal Microbiome Diversity Following Intranasal Mupirocin Treatment
Johns Hopkins University · NCT06805994
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 0 mo–60 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 1
- Target enrollment
- 175
- US sites recruiting
- 1
- Study start
- August 27, 2025
- Record last updated
- August 10, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This protocol aims to evaluate how NMT affects pediatric nasal microbiome diversity following intranasal mupirocin treatment
Being studied: Nasal Microbiota Transplant (NMT); Placebo
Conditions: Staphylococcal Aureus Infection; Microbial Colonization; Pediatric Infection; S. Aureus Colonization; Microbial Transplant
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Child
Inclusion criteria
- Child has had a prior nasal surveillance culture grow S. aurues
- Child is \<18 years of age
- Child completed treatment with intranasal mupirocin for S. aureus nasal colonization as part of routine clinical care two or more days before the planned transplant
- Child has anticipated hospital length of stay >3 days after completing intranasal mupirocin treatment
- Infant >25 weeks gestation unless >2 months chronological age
Exclusion criteria
- Child is a ward of the State
- Child with a diagnosis of immunodeficiency or antenatal suspicion for immunodeficiency (e.g., sibling with known immunodeficiency, genetic syndrome with known associated immunodeficiency)
- Child cannot have nasal swabs collected (due to anatomic or other clinical intervention, including nasal packing)
Donor
Inclusion criteria
- Donor is able to provide informed consent
- Donor has a relationship with the child outside of the hospital setting (i.e., not an ICU caregiver)
Exclusion criteria
- Donor had positive COVID-19 test in prior 21 days
- Donor with signs or symptoms of respiratory illness (e.g. runny nose, congestion, fever, cough)
- Donor has been in close contact with someone in the last 7 days who had a respiratory viral infection (e.g., cold, flu)
- Donor tests positive on baseline screening test for S. aureus nasal colonization.
- Donor tests positive on baseline screening test for a respiratory pathogen.
- Donor is not able to provide written informed consent
- Donor is not able to be present at the bedside at the time of intervention.
- Donor has history of chronic sinusitis, cystic fibrosis, or an infection with a multi-drug resistant organism.
- Inability or unwillingness to complete the Donor questionnaire or a positive response to any question on the Donor questionnaire.
- Donor has smoked within the last month
Recruiting US locations
Johns Hopkins University
Baltimore, MD 21287
Site contact: Danielle Koontz, Research Manager · 443-287-9040 · dkoontz1@jhmi.edu
Study contacts (from the official record)
- Danielle Koontz, Research Manager · 4432879040 · dkoontz1@jhmi.edu
- Slade Decker, Senior Research Coordinator · 4109550405 · sdecker9@jhmi.edu
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