10-Year checkup: does this tooth repair material last?
NCT ID NCT05084742
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at how well a dental material called Biodentine™ performs 10 years after being used for root repairs, such as fixing holes or filling the tip of a root. Researchers will check X-rays and do exams on 145 patients who had these treatments. The goal is to see if the treatment is still successful and safe over the long term.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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145 people
The number who actually took part.
- Started
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Nov 2021
- Expected to finish
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Sep 2033
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
160 patients with a permanent tooth treated at least 1 year and no more than 5.5 years ago through an endodontic microsurgery using Biodentine™, all microsurgery including root end-filling, external or internal root resorption repair, root and furcation perforation repair, apexification, and revitalization procedure by means of revascularization.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Male or female, adult or child with permanent study tooth (immature or mature) * Study tooth treated with an endodontic microsurgery using Biodentine™: all microsurgery including root end-filling, external or internal root resorption repair, root and furcation perforation repair and apexification * Study tooth treated at least 1 year and no more than 5.5 years before inclusion visit * Availability of baseline radiographic image of the study tooth * Patient affiliated to national health insurance * Patient informed about the study and who confirms his/her consent to participate to the study Exclusion Criteria: * Patient treated with anti-cancer therapy in the 5 years prior to the treatment * Uncontrolled systemic disease 1 month prior to the treatment * Development of a cancer or a systemic disease just after the treatment * Participation to an interventional clinical trial at the time of the treatment
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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AP-HP, Hôpital Louis Mourier
Colombes, France
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CHU de Nantes
Nantes, France
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CHU de Reims
Reims, France
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CHU de Toulouse
Toulouse, France
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HCL de Lyon
Lyon, France
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Private dental care office
Paris, France
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Other studies related to the condition(s) this trial covers.
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