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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03660163
Other study ID # 08/H0804/79 v.3
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date November 1, 2016
Est. completion date August 1, 2019

Study information

Verified date August 2018
Source King's College London
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the study is to assess the correlation between pre-obturation bacterial detection using fluorescence amplification and outcome of endodontic treatments. Thus, enabling a suitable detection threshold to predict the likelihood of treatment failure. This has the potential to be used a bench side tool in general dental practice to act as a surrogate endpoint for clinicians performing root canal treatment.


Description:

Pre-obturation root canal samples were taken using paper points from patients undergoing primary root treatments. The samples were analyzed using a fluorescent spectrometer and a molecular fluorescent vital dye (Calcein AM).

Pre-operative and 1-year post-operative periapical radiographs and Cone Beam Computed Tomography (CBCT) scans were assessed by two calibrated expert examiners to evaluate the outcome of the root canal treatments.

The use of a chairside bacterial stain can allow the clinician to predict the outcome of treatment with confidence. Sampling the root canal space with endodontic paper points followed by ex-situ fluorescent staining and analysis provides a patient-friendly, simple to use and rapid way of predicting root canal treatment outcome.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 65
Est. completion date August 1, 2019
Est. primary completion date August 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with at least one tooth diagnosed with the endodontic disease.

- teeth that were tender to percussion and palpation.

- teeth that had a sinus tract and/ swelling.

- Both primary treatment teeth and teeth which had already been root treated were considered.

Exclusion Criteria:

- Patients were excluded if they were pregnant.

- Immunosuppressed patients.

- Non-restorable teeth.

- Teeth with a periodontal probing depth greater than 3mm.

- Teeth with apical radiolucencies with the longest dimension above 1.2cm.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
King's College London

Outcome

Type Measure Description Time frame Safety issue
Primary Periapical periodontium health Assess the health of periapical periodontium of a tooth by examining the CBCT image One year
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