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Oropharyngeal Candidiasis (OPC) and S-ECC

Association Between Early Candida Infection (Oral Thrush) and Severe Early Childhood Caries (S-ECC)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05761197
Acronym
Oral-Thrush
Enrollment
70
Registered
2023-03-09
Start date
2024-09-01
Completion date
2028-08-31
Last updated
2026-06-22

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

Conditions

Candida Infection, Early Childhood Caries, Oral Thrush

Keywords

Oral candidiasis, Candida infection, Oral thrush, Early childhood caries, Oral Health

Brief summary

The overall objective of this study is to investigate the association of early Candida infection (known as oral thrush or oropharyngeal candidiasis, OPC) in children during the first year of life with the onset and severity of severe early childhood caries (S-ECC).

Detailed description

The overall goal of this study is to conduct a longitudinal observational study to investigate the association of early OPC with the onset and severity of S-ECC to better understand the role of Candida (particularly C. albicans) in severe childhood caries. The investigators will test the hypothesis that OPC is associated with S-ECC by modifying the plaque microbiota and enhancing virulence in a manner that is conducive to the early development of the disease. For this study, a total of 70 infants (aged 9-15-month-old) with or without a history of OPC in their first year of life will be enrolled, based on the inclusion and exclusion criteria. Subjects will have their medical/dental history reviewed from medical records. At each study visit (Baseline, 6-month, 12-month, 18-month, and 24-month follow-ups), an oral examination including soft tissue and caries exam will be performed by a calibrated evaluator. Dental plaque/oral swab samples will be collected at each study visit. In addition, a comprehensive survey including demographic status, oral hygiene, diet, delivery, and feeding method as well as current medication usage will also be collected.

Interventions

None listed

Sponsors

Temple University
Lead SponsorOTHER
Children's Hospital of Philadelphia
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
9 Months to 15 Months
Healthy volunteers
Yes

Inclusion criteria

* Male or female individuals at the age of 9-15-month-old * Must have at least one fully erupted tooth at baseline visit * Parent/guardian willing and able to provide informed consent * With or without a history of OPC (the study team will enroll 35 participants with and 35 participants without a history of OPC)

Exclusion criteria

* Presence of a systemic medical condition (e.g. Down syndrome etc.) * Presence of an orofacial deformity * Presence of dental caries * Use of systemic antimicrobial therapy within 30 days of the baseline visit * Presence of any condition which, in the opinion of the investigator, makes participation in the project not in the individual's best interest.

Design outcomes

Primary

MeasureTime frameDescription
To explore the association between OPC and S-ECC onset and severity24 monthsCaries will be measured by ICDAS scoring system; Plaque and oral swab samples will be collected at each study visit (Baseline, 6-month, 12-month,18-month and 24-month follow-ups); Candida strains will be detected using culturing-dependent and -independent sequencing techniques.

Secondary

MeasureTime frameDescription
To evaluate the influence of OPC on the oral microbiota24 monthsMicrobiome profiling will be done by shot gun sequencing

Countries

United States

Contacts

CONTACTYuan Liu, DDS, MS, PhD
yuan.liu0008@temple.edu215-707-8029
PRINCIPAL_INVESTIGATORYuan Liu, DDS, MS, PhD

Temple University Kornberg School of Dentistry

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 23, 2026