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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03281746
Other study ID # MCC-16-13019
Secondary ID NCI-2017-01354
Status Terminated
Phase N/A
First received
Last updated
Start date May 19, 2017
Est. completion date March 2, 2018

Study information

Verified date February 2020
Source Virginia Commonwealth University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This randomized pilot clinical trial studies how well preventive education works in decreasing caries formation in pediatric patients with leukemia. Prevention education may have an effect on factors important in causing cavities in pediatric patients with leukemia.


Description:

Patients treated for leukemia at Virginia Commonwealth University Medical Center in the department of Pediatric Hematology and Oncology are currently receiving oral hygiene instruction at diagnosis. In this study, patients will be randomized into two groups at diagnosis: one receiving current prevention education and the other group receiving one-on‐one prevention education and counseling with the physician and pediatric dental resident. Physician and pediatric dental resident will use motivational interviewing informed techniques during counseling. A caries risk assessment will be performed for each patient at diagnosis. Caries incidence, plaque scores, mutans streptococci levels, salivary flow rate, and salivary pH will be assessed at week one (diagnosis), week 16 or start of interim maintenance therapy whichever comes second, week 32 or beginning of maintenance therapy whichever is later for all patients enrolled in the study. Data will be collected through a clinical intraoral examination and salivary sample. Data collected will be used to assess the effect of increased prevention education on factors of importance in caries formation.


Recruitment information / eligibility

Status Terminated
Enrollment 2
Est. completion date March 2, 2018
Est. primary completion date March 2, 2018
Accepts healthy volunteers No
Gender All
Age group 3 Years to 12 Years
Eligibility Inclusion Criteria:

- Pediatric patients who have been recently diagnosed with leukemia

- Patients will also predictably be in primary or mixed dentition

- Patients of Virginia Commonwealth University Medical Center Pediatric Hematology Oncology Clinic

Exclusion Criteria:

- Full permanent dentition

- Primary language is not English

- Children in the custody of the state with no parent or legal guardian present to sign consent

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Dental Procedure
Undergo dental examination
Other:
Educational Intervention (prevention education)
Receive prevention education
Interview
Ancillary studies
Survey Administration
Ancillary studies
Educational Intervention (one-on one education)
Receive one-on-one education

Locations

Country Name City State
United States Virginia Commonwealth University/Massey Cancer Center Richmond Virginia

Sponsors (2)

Lead Sponsor Collaborator
Virginia Commonwealth University National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in caries assessed by CAMBRA risk assessment tool Baseline up to 32 weeks
Primary Change in salivary flow rate Change in salivary flow rate will be measured utilizing pre-weighed cotton rolls. Patients will saturate as many cotton rolls as possible in one minute by chewing. Dose cups and cotton rolls will be weighed prior to and after data collection. The change in weight in grams will be converted to mL of saliva collected. Baseline up to 32 weeks
Primary Change in salivary pH Will be measured with litmus paper in the gingival sulcus of the tooth where plaque is collected for bacterial load testing. Baseline up to 32 weeks
Primary Change in levels of mutans streptococci in buccal surface of most posterior maxillary right tooth Samples will be plated on mitis salivarius and incubated. Mutans streptococci colonies will be counted after incubation. Baseline up to 32 weeks
Primary Change in caries assessed by Merged International Caries Detection and Assessment System (ICDAS) Baseline up to 32 weeks
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