Prospective Endodontics Database

• Conditions: Apical Periodontitis

• Registration Number: NCT04716478
• Lead Sponsor: Hospices Civils de Lyon

Brief Summary

Endodontic treatment is necessary after certain dental trauma or in the presence of a large carious lesion, associated with signs of irreversible pulpal inflammation. The treatment of apical periodontitis is a real public health issue. The endodontic success rate is between 68 and 85%. Indeed, some studies show that systemic diseases such as diabetes can increase the prevalence and bone loss associated with apical periodontitis. Other studies identify apical periodontitis as a factor that can potentiate symptoms caused by inflammatory diseases such as cardiovascular disease and diabetes by increasing the level of inflammatory cells in the blood.

However, since 2014 the European Society of Endodontology has recommended establishing a higher level of evidence to ensure the link that these pathologies may have. For this, it is necessary to assess the criteria that may influence the healing of apical periodontitis.

Endodata has been developed by dental surgeons specializing in endodontics. The purpose of this software is to improve the clinical follow-up of patients and to establish a clinical and radiological database. In this context, the creation of a clinical database including data for all root canal treatment is of high interest.

Detailed Description

Not available

Study Timeline

• Status Verified: 2021-01
• Study First Submitted: 2021-01-15
• Study First Submitted QC: 2021-01-15
• Study First Posted: 2021-01-20
• Study Start: 2021-01-22
• Last Update Submitted: 2021-05-05
• Last Update Posted: 2021-05-06
• Primary Completion: 2022-06-01
• Study Completion: 2023-06

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 400

Inclusion Criteria

• Adult patient aged ≥ 18,
• New patients received in consultation by students registered for a Diploma in Endodontics in one of the participating centres (Brest, Bordeaux, Lyon, Nancy, Nantes, Nice, Paris, Toulouse) or received by one of the private practitioners participating in the study;
• Patient with an indication for endodontic treatment or endodontic retreatment on at least one permanent tooth.

Exclusion Criteria

• Patient unable to understand the purpose and conduct of the study.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The main objective is to build a database with the necessary, relevant and quality data that will allow the development of a diagnostic and therapeutic aid in endodontics.	follow-up at 6 months.	The patient's medical pathologies, the results of tests and clinical examination, radiological analysis and diagnostics is recorded during routine care. The treatment protocol is detailed for each technique, product or material used.

Trial Locations

Locations (21)

CHU de Bordeaux, Service de Médecine Buccodentaire; 🇫🇷 Bordeaux, France

CHU de Brest, Service d'Odontologie; 🇫🇷 Brest, France

Cabinet du Dr Baptiste Rivory; 🇫🇷 Lyon, France

Cabinet du Dr Matthieu Durand; 🇫🇷 Lyon, France

Cabinet du Dr Oussama Bouamar; 🇫🇷 Lyon, France

Cabinet du Dr Paul-Marie Oliva; 🇫🇷 Lyon, France

Hospices Civils de Lyon, Service d'Odontologie; 🇫🇷 Lyon, France

UFR d'Odontologie, Laboratoire des Multimatériaux et Interfaces; 🇫🇷 Lyon, France

CHRU de Nancy, Service d'Odontologie; 🇫🇷 Nancy, France

CHU de Nantes, Service d'Odontologie; 🇫🇷 Nantes, France

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