Feasibility of the Preparation of an Advanced Therapy Medicinal Product for Dental Pulp Regeneration

Completed

• Conditions: Dental Pulp Regeneration; Dental Stem Cells
• Interventions: Other: teeth avulsion

• Registration Number: NCT02842515
• Lead Sponsor: Centre Hospitalier Universitaire de Besancon

Brief Summary

Current endodontic treatment are based essentially on the ouster of parenchyma in case of trauma or irreversible pulp inflammation. These situations typically affect immature teeth in subjects aged from 8 to 15 years. Consequently, loss of a functional pulp is leads to discontinuation of root development and apical closure. The challenge for the clinician in the management of such situations is then preserving a pulp vitality. But current practices consist in a filling of the endo-canal system with an inert or semi-inert material. In this case, no pulp vitality is present. New treatment methods are needed. The objective Pulp'R is the study the feasibility of preparing an autologous combined advanced therapy medicinal product (ATMP) for dental pulp regeneration in the patient with irreversible pulp inflammation or dental trauma.

Detailed Description

Not available

Study Timeline

• Study Start: 2015-01
• Primary Completion: 2015-07
• Study Completion: 2015-07
• Status Verified: 2016-07
• Study First Submitted: 2016-07-18
• Study First Submitted QC: 2016-07-20
• Last Update Submitted: 2016-07-20
• Study First Posted: 2016-07-25
• Last Update Posted: 2016-07-25

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Patients aged from 8 to 15 years, with at least one tooth affected by a carious process,
• Patients aged from 8 to 15 years with major trauma preventing the maintenance of the tooth in the arch
• Patients aged from 16 to 20 years requiring avulsion germs wisdom teeth,
• Ability to carry out the extraction of pulp chamber content
• Signature of informed consent (from the patient and his guardian)
• Indication that the subject has understood the purpose and procedures required by the study and agrees to participate in the study and comply with the requirements and limitations inherent in this study,
• Patient with French social insurance.

Exclusion Criteria

• Lack of ability to collect the dental pulp,
• Presence of necrosis in pulp complex or the possibility of preserving the pulp through appropriate techniques,
• Legal incapacity or limited legal capacity
• Patient unlikely to cooperate in the study and / or low cooperation anticipated by the investigator,
• Patient without health insurance,
• The patient is in the period of exclusion of another study,
• Patients with congenital pathology of dental pulp (amelogenesis and dentinogenesis imperfect)
• Patient with intrapulpal calcification or violations of pulp obliteration
• Teeth having external or internal inflammatory resorption
• Teeth diagnosed with pulp necrosis process
• Teeth undergoing fragmentation for their avulsion
• Time of pulp air exposition > 2 hours (risk of bacterial contamination)

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Patients requiring dental avulsion	teeth avulsion	Patients requiring dental avulsion

Primary Outcome Measures

Name	Time	Method
Number of stem cell lines established from pulp removed during either traumatic or carious teeth avulsion	1 day