Diagnosis Dual, Trauma
Conditions
Keywords
Laser Doppler flowmetry, pulpal blood flow, pulp vitality, traumatised teeth, paediatric dentistry
Brief summary
The aim of the study is to evaluate the efficacy of Laser Doppler flowmetry in determining the changes in the pulpal blood flow during the post-traumatic period of traumatised permanent teeth.
Detailed description
Traumatic injuries of permanent teeth in children and adolescents are very common. The conventional pulp vitality tests are inaccurate and unreliable techniques in assessing the pulp vitality during the post-traumatic period, as well as during the immature teeth examination. The aim is to evaluate the efficacy of Laser Doppler flowmetry in determining the changes in the pulpal blood flow during the post-traumatic period of traumatised permanent teeth. The study is designed as a randomized, split-mouth, controlled clinical trial. The measurement of the blood flow of the dental pulp of both, traumatised and non-traumatised teeth, will be performed, using a laser doppler flow monitor, emission wavelength 785nm±10nm, dual-channel laser Doppler monitoring option.
Interventions
DIAGNOSTIC_TESTMeasurement of pulpal blood flow of traumatised tooth
Measurement of the blood flow of the dental pulp will be performed, using a laser doppler flow monitor mVMS-LDF2TM (Moor Instruments Ltd Millwey Axminster Devon, UK), emission wavelength 785nm±10nm, dual-channel laser Doppler monitoring option. Two probes will be used, each consisting of one afferent and one efferent optic fiber to conduct the light to and from the tooth surface. The probe is stainless steel needle-like tube, which is 10-80 mm long and 1.5 mm in the diameter. The utilised parameter settings will be: Average power - 1.0 mV; Diameter of the probe - 1.5 mm; Frequency - 40 Hz; Monitoring time-180 seconds (sec)
Sponsors
Plovdiv Medical University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE
Intervention model description
a randomized, split-mouth, controlled, clinical trial
Eligibility
Sex/Gender
ALL
Age
No minimum to 18 Years
Healthy volunteers
Yes
Inclusion criteria
1. Fit and healthy subjects aged \< 18-year-old; 2. Subjects with maxillary permanent incisor subjected to a traumatic injury without any dentoalveolar trauma involvement and have a contralateral homologous tooth with no signs/symptoms of injury; 3. Subjects attended their first dental visit within 3 days of the dental trauma; 4. Sensitivity value of the electric pulp test over 200 μA; 5. Subjects with at least one vital and non-traumatised maxillary incisor acting as a control tooth; 6. Ability to obtain a verbal acceptance from all the subjects to comply with all the treatments and follow-up timepoints attendance; 7. Ability to obtain written informed consent by the patients' parents/guardians for treatment, participation in the study and publication
Exclusion criteria
1. Subjects who were undergoing therapy for neurological conditions or with mental or cognitive problems; 2. Subjects who were taking sedative, analgesic, and/or anti-inflammatory medication 7 days prior to the treatment commencement; 3. Subjects who have never had any first dental visit or treatment; 4. Subjects with systemic diseases or physiological development delay; 5. Subjects with active infectious diseases such as; influenza, scarlet fever, etc. 6. Subjects with restorations covered more than half the labial surface of the investigated teeth.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in pulpal blood flow | 180 seconds | The traumatised and non-traumatised teeth, test and control, will be assessed by LDF, providing an accurate and precise investigation. The temperature in the dental office will be constant and the patient will be seated in a state position in the dental chair. According to the manufacturer's recommendations, a patient's relaxation of 10 minutes before the monitoring process will be obtained. The measurements of blood flow will be performed for 180 seconds at each session. All the measurements will be recorded. |
Countries
Bulgaria
Contacts
Primary ContactMaria Shindova, PhD
Backup ContactAni Belcheva, PhD
Outcome results
None listed