The Adjunctive Effect of Soft Tissue Augmentation Procedures of Moderate-severe Peri-implantitis
Recruiting
N/A
Interventional Study
Peri-Implantitis
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 120 (estimated)
- Sponsor
- Nadja Naenni · Other
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About This Trial
The key objective of the study is to compare the effects of soft tissue augmentation using a volume stable collagen matrix or autogenous connective tissue graft or no soft tissue augmentation in addition to bone grafting/implantoplasty in patients who undergo surgical therapy of peri-implantitis with respect to clinical resolution of the infection.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Age \> 18 years old (UZH, FRA) or \> 21 years old (SIN), male and female.
2. Diagnosed with periimplantitis of at least 1 implant in function for at least 1 year Diagnostic criteria
* Presence of bleeding and/or suppuration on gentle probing.
* Probing depths of ≥6 mm.…
Contacts