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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03005197
Other study ID # 1
Secondary ID
Status Not yet recruiting
Phase N/A
First received December 22, 2016
Last updated January 4, 2017
Start date February 2017
Est. completion date May 2018

Study information

Verified date January 2017
Source University of Leeds
Contact Nahar Ghouth, BDS
Phone 0113 343 6228
Email dnnng@leeds.ac.uk
Is FDA regulated No
Health authority United Kingdom: National Health Service
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date May 2018
Est. primary completion date May 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 6 Years to 16 Years
Eligibility 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.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Device:
Laser Doppler Flowmetry


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Leeds

References & Publications (1)

Jafarzadeh H. Laser Doppler flowmetry in endodontics: a review. Int Endod J. 2009 Jun;42(6):476-90. doi: 10.1111/j.1365-2591.2009.01548.x. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Sensitivity One year follow up No
Primary Specificity One year follow up No
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