Timing of dental implant repair could be key to saving smiles
NCT ID NCT07325747
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether waiting a bit before surgically repairing bone damage around infected dental implants leads to better results than fixing it right away. Forty adults with peri-implantitis (gum infection around implants) will be randomly assigned to one of two surgical approaches. The goal is to see which method improves bone healing and patient comfort more effectively.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2026
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- 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: * Systemically healthy adults * Age ≥ 18 years * The patient must be able to perform good oral hygiene * With at least one implant with either cement or a screw-retained prosthesis demonstrating a diagnosis of peri-implantitis at an implant in function for a minimum of 1 year with a prosthesis installed. * In cases where previous radiographic records are available: presence of bleeding and/or suppuration on gentle probing, increased probing depth compared to previous examinations, and radiographic evidence of bone loss beyond initial crestal remodeling. (Berglundh 2018). * In cases where baseline radiographs are not available: presence of PPD ≥6 mm with BOP and/or suppuration (SUP) and radiographically detectable marginal bone loss (MBL) exceeding 3 mm on an implant in function forfor at least 1 year (Berglundh 2018). * Target implants have to also demonstrate the presence of a peri-implant intra-bony defect with a depth ≥3 mm and width ≤4 mm, as assessed on radiographs and confirmed intra-surgically. In addition, the bony defect should present with a minimum of two walls . No implant mobility and no evidence of occlusal overload. In patients presenting with more than one implant meeting the inclusion criteria, a single implant will be randomly selected for inclusion in the study. Exclusion Criteria: * Short implants (≤ 6mm) * Contraindications for undergoing oral surgery. * Patients pregnant or attempting to get pregnant (self-reported), or nursing women. * Untreated/active periodontitis, or other untreated acute infections at the surgical site. * Untreated malignancies at the surgical site. * Self-reported current smoking, or active tobacco chewing, or chronic vaping. * Taking long-term (\>1yr) NSAID, prednisone or other anti-inflammatory prescription drugs * Patients with any known history of blood disorders or complications such as abnormal concentration of thrombin and factor XIII in plasma, or hemophilia. * Patients with significant co-morbidities, such as obesity, uncontrolled diabetes, immunosuppression, severe endocrine-induced bone diseases, signs of malnourishment, those receiving immunosuppressive therapy, poor tissue oxygenation or perfusion, and pre- or post-operative radiation. * Unable to give consent for participation.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Michigan School of Dentistry
RECRUITINGAnn Arbor, Michigan, 48109, United States
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Other studies related to the condition(s) this trial covers.
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- Could tiny metal shavings from dental implants fuel gum disease?
- Could your bone health decide if a dental implant lasts?