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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04186065
Other study ID # 47148
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2019
Est. completion date October 31, 2019

Study information

Verified date June 2020
Source University of Kentucky
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study investigates how often cavities develop on the permanent teeth of patients with braces (orthodontic treatment). The hypothesis is that there is no difference in the number of cavities on the permanent teeth of patients with braces compared to similar patients without braces.


Description:

The purpose of this cross-sectional study is to determine the prevalence of early carious lesions (white spot lesions, or WSLs) for patients who are receiving orthodontic treatment compared to patients who are not receiving orthodontic treatment.

Subjects will be recruited from the University of Kentucky Orthodontic Clinic patient pool. Orthodontic care at the University of Kentucky College of Dentistry (UKCOD) is provided by orthodontic faculty, as well as students enrolled in the graduate orthodontic program at the UKCOD. Subjects will be invited to participate in this study after receiving an initial treatment plan with fixed appliances for at least one arch.


Recruitment information / eligibility

Status Completed
Enrollment 111
Est. completion date October 31, 2019
Est. primary completion date October 31, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 10 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients who agreed to participate in this study

- Patients who receive orthodontic treatment with fixed appliances at University of Kentucky College of Dentistry

- Patients who have either metal or ceramic brackets for the treatment

Exclusion Criteria:

- Patients on a daily supplemental fluoride regimen

- Patients who has difficulty in their daily toothbrushing due to their physical disability

- Patients with lingual fixed appliances

- Patients who are pregnant

- Patients with restorations placed on the facial/buccal surface of the tooth from premolar to premolar for both arches.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Kentucky College of Dentistry Lexington Kentucky

Sponsors (1)

Lead Sponsor Collaborator
Hiroko Nagaoka

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The formation of early caries lesion on teeth (white spot lesions) Teeth of study subjects will be evaluated for the formation of white spot lesions based on their intraoral photographs taken at their participation for the study. One-time assessment at participant visit (approximately 30 minutes).
Primary The dental plaque deposit on teeth. Teeth of study subjects will be stained with the plaque disclosing agent. After rinsing off the disclosing agent, intraoral photographs are taken for later analysis of dental plaque accumulation. One-time assessment at participant visit (approximately 30 minutes).
Primary Subjects' of attitude toward the oral hygiene practice. Participants will be asked to take an electronic questionnaire (through REDCap) consisting of 13 items that assess their dental hygiene practice and attitude toward orthodontic treatment. Individual question responses range from 0-7 (cumulative range of 0-91) with higher scores indicating more positive attitudes. One-time assessment at participant visit (approximately 30 minutes).
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