Reconstructive surgical therapy of peri-implantitis-related osseous defects. a multicenter randomized controlled clinical trial
NCT ID NCT03077061
First seen Sep 10, 2026 · Last updated Sep 10, 2026
Summary
The project will evaluate the potential benefit of the use of bone replacement graft as an adjunct to surgical therapy of peri-implantitis. The project will be conducted as a two-armed randomized controlled clinical trial of 5-year duration in 7 clinical centers. 140 systemically healthy patients diagnosed with peri-implantitis will randomly assigned to be treated with or without bone replacement graft. Outcome measures include assessments of inflammation, probing depth, recession, radiological parameters and PROMs.
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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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140 people
The number who actually took part.
- Started
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Apr 2017
- Expected to finish
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Nov 2026
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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥ 18 years * ≥1 implant (≥1 year of function) presenting with PPD ≥7 mm and BoP/Pus. * Confirmed bone loss ≥3 mm at same implant(s) Exclusion Criteria: * Treated for peri-implantitis during previous 6 months * Intake of systemic or local antibiotics during previous 6 months * Systemic conditions affecting peri-implant tissues * Systemic conditions impeding surgical intervention
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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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Department of Periodontology, Institute of Odontology
Gothenburg, 40530, Sweden
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Implant survival after reconstructive surgical therapy of peri-implantitis-related bone defects with different defect configurations
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