- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05648305
The Influences of Root Canal Complexity and Clinician Training on Root Canal Treatment Outcomes.
Root Canal Treatment is a Common Intervention for Military Patients Suffering From- or at Risk of Suffering From- Endodontic Disease. This Retrospective Cohort Study Assesses the Influence of (a) Root Canal Complexity Using the Restorative Index of Treatment Need (RIOTN) Index and (b) Operator Skill (Clinicians Who Had Received Additional Post-graduate Root Canal Treatment Training, on Survival (Tooth Present at End of Study Period) and Success (Radiographic Apical Healing) of Root Canal Treatment
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Background and Study Aims. This observational cohort study evaluates root canal treatment outcomes, using survival and success as the outcome measures. It aims to assess the influence of operator skill and RIOTN complexity on the clinical outcomes of RCT procedures previously undertaken within the UK Armed Forces.
Participation UK Armed Forces personnel that had previously received root canal treatment between 01/01/2015 and 01/09/2020.
Method
A Defence Statistics programme was used to identify cohorts of patients treated for Endodontic disease by GDPs and DWSI (GDPs who had undertaken a 1 year post-graduate training programme in Endodontics). The researcher group was calibrated to the study's method and this was initially piloted on 5 patient records, with further calibration undertaken until researcher consistency was achieved via inter-operator reliability testing. The researchers subsequently reviewed 1600 patient records, eventually establishing a cohort of 1267 patients (580 - Group 1 (GDP) and 687 - Group 2 (DWSI). The clinical records and radiographs of these groups were reviewed for the following:
1. Tooth survival 2. RIOTN complexity at the time of treatment 3. RCT success (apical healing). Secondary factors assessed included: age, gender, smoking status, diabetic status, steroid status, presence of an indirect restoration, presence of a post, reasons for tooth loss (if tooth did not survive).
The collection of data has now been completed and is ready for analysis.
Risks and Benefits This study will benefit Defence Primary HealthCare and UKAF personnel as it will influence and shape future care provision for Endodontic disease within the military. There are no identified risks of participation.
Study Location The study is being run from the Defence Centre for Rehabilitative Dentistry, Evelyn Woods Road, Aldershot, GU11 2LS. The study is evaluation the outcomes of clinical practitioners working within the 200+ Dental Centres within the UK and overseas locations.
Funding There is no established funding for this study. There are no commercial or other conflicts of interest.
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Served/ were serving within the UK Armed Forces.
- Male and female.
- Physically able to tolerate root canal treatment/ re-treatment procedures.
- Received root canal treatment/ re-treatment for Endodontic disease by either a GDP or Dentist with Specialist interest (DWSI).
- Aged between 18 - 70..
- 12-month (or longer) post root canal treatment review radiograph and consultation.
- Smoking and non-smoking patients
- With and without Diabetes Mellitus 2
- Taking/ not-taking steroid medications
- With/ without other medical conditions.
Exclusion Criteria:
- On longer serving in the military within 12-months of root canal treatment completion.
- Unable to tolerate root canal treatment/ re-treatment
- No clinical follow-up of tooth (survival).
- No radiographic follow-up of tooth (success).
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
General Dental Practitioners
Cohort 1 consisted UK Armed Forces Personnel that received root canal treatment within the study period by General Dental Practitioners.
|
The provision of Root Canal Treatment for teeth with Endodontic infection or to prevent Endodontic infection.
Other Names:
|
|
Dentists with Specialist Interest (DWSI)
Cohort 2 consisted UK Armed Forces Personnel that received root canal treatment within the study period by DWSI, clinicians that had undertaken a 1-year post-graduate programme in Endodontics.
|
The provision of Root Canal Treatment for teeth with Endodontic infection or to prevent Endodontic infection.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
1. Tooth survival
Time Frame: 6-months - 48-months post-treatment.
|
Tooth still present in the mouth at end of trial period.
|
6-months - 48-months post-treatment.
|
|
2. Root Canal Treatment Success
Time Frame: 6-months - 48-months post-treatment.
|
The absence of signs, symptoms and evidence of radiographic peri-apical radiolucency resolution.
|
6-months - 48-months post-treatment.
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: Neil MacBeth, BDS PhD, Defence Primary Healthcare
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- DefencePHC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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