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Frequent Standardized Oral Care to Improve Health Outcomes in Premature Infants in the Neonatal Intensive Care Unit

Frequent Standardized Oral Care to Improve Health Outcomes in Premature Infants in the Neonatal Intensive Care Unit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05167318
Enrollment
150
Registered
2021-12-22
Start date
2022-01-15
Completion date
2026-10-30
Last updated
2026-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Microbial Colonization, Ventilator Associated Pneumonia

Brief summary

Premature very low birth weight (VLBW) infants are susceptible to complications related to infrequent and non-standardized oral care. Although the benefits of frequent standardized oral care are known to reduce oral dybiosis (increased level of potentially pathogenic bacteria) and its associated complications in critically ill adults leading to established evidence-based guidelines, no such information exists for VLBW infants. The proposed study will prospectively follow 40 VLBW infants for 4 weeks following birth. Infants will be randomized into 1 of 2 groups. Standardized oral care will be performed every 3-4 hours (Group 1) and every 12 hours (Group 2). Aim 1 will evaluate the feasibility of frequent standardized oral care, Aim 2 will compare the oral microbiome between groups, and Aim 3 will compare respiratory outcomes including the incidence of ventilator associated pneumonia, bronchopulmonary dysplasia and need for respiratory support between infants receiving standardized oral care every 3-4 hours and every 12 hours. Issues related to recruitment, retention, randomization, acceptance by nursing staff, and treatment fidelity will be examined. Saliva samples will be obtained weekly and analyzed using 16S sequencing, respiratory cultures will be obtained weekly on ventilated infants, and respiratory outcomes will be collected from the medical records.

Interventions

OTHERfrequent standardized oral care

Standardized oral care will be provided every 3-4 hours

Sponsors

University of Florida
Lead SponsorOTHER
National Institute of Dental and Craniofacial Research (NIDCR)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
12 Years to 72 Years
Healthy volunteers
No

Inclusion criteria

* Gestational age \< 32 weeks * birth weight \< 1500 grams * mother is English speaking * mother is \> 18 years of age.

Exclusion criteria

* Congenital anomalies of the face, lungs, or gastrointestinal system * not expected to survive

Design outcomes

Primary

MeasureTime frameDescription
Type of of bacterial in the oral cavityweekly for 4 weeksmicrobial analysis of the oral microbiome

Secondary

MeasureTime frameDescription
Days of respiratory supportUp to 100 daysnumber of days infant was on respiratory support
Incidence of chronic lung diseaseUp to 100 daysWhether or not the infant was diagnosed with chronic lung disease

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORLeslie Parker

University of Florida

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 19, 2026