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Laser Doppler Flowmetry in Assessing the Vitality of Traumatised Teeth

A Prospective Study to Assess the Diagnostic Accuracy of Laser Doppler Flowmetry in Assessing Pulp Vitality of Traumatised Teeth in Paediatric Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03005197
Enrollment
30
Registered
2016-12-29
Start date
2017-02-28
Completion date
2018-05-31
Last updated
2017-01-05

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

Conditions

Dental Trauma

Brief summary

Teeth injuries are considered one of the most challenging events that occur in dentistry, especially in children. After an injury, there is a possibility that the blood supply to the tooth may become affected and compromised leading to nerve and blood vessels death with the tooth described as a non-vital tooth. The conventional diagnostic tools available to assess tooth nerve/blood supply are not always reliable. Child cooperation and understanding contribute greatly to this shortfall. Failure to assess the vitality of the tooth may result in pain, swelling or infection of the tooth or de-vitalising a normal tooth which may render the tooth weak for the future and possibly losing the tooth. The laser Doppler flowmetry is a non-invasive, non-painful technique and shown to be more reliable than the traditional techniques. We aim to assess if this device can predict and assess whether the tooth is alive or dead during the follow up visits of the injury along the other conventional tests.

Detailed description

A clinical study will be carried out which consists of a one year follow up to monitoring traumatised front teeth in children attending the department of paediatric dentistry. The vitality/sensibility of traumatised teeth will be assessed using laser Doppler flowmetry, electrical pulp testing and ethyl chloride. Measurements will be performed by a single operator (chief investigator) and will be carried out at baseline, 3, 6, 9 and 12 months follow up period.

Interventions

Sponsors

University of Leeds
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
6 Years to 16 Years
Healthy volunteers
Yes

Inclusion criteria

Children would be recruited into this study when they: * Between 6-16 years old. * Medically fit (ASA I, II). * Able to communicate using English language. * Have an acceptable level of cooperation. * Have at least one traumatised anterior tooth, regardless of the type of trauma, with uncertain pulpal vitality requiring monitoring for a minimum of 12 months and minimal coronal restoration (covering less than half the labial crown surface). * Have at least one vital and non-traumatised anterior tooth to act as a control.

Exclusion criteria

* Medically and mentally compromised children. * Children with learning disabilities. * Children with communication barrier including those unable to communicate using English language. * Heavily restored teeth covering more than half the labial surface of teeth. * Patients on routine analgesics, antidepressants or antihypertensive drugs. * Vital teeth with pulp canal obliteration.

Design outcomes

Primary

MeasureTime frame
SensitivityOne year follow up
SpecificityOne year follow up

Contacts

Primary ContactNahar Ghouth, BDS
dnnng@leeds.ac.uk0113 343 6228

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026