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Administering NMT to Reestablish Infant Nasal Microbiome Diversity Following Intranasal Mupirocin Treatment

Johns Hopkins University · NCT06805994

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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
Administering NMT to Reestablish Infant Nasal Microbiome Diversity… (NCT06805994) | Bored Studies