Actively Recruiting
The Adjunctive Effect of Soft Tissue Augmentation Procedures of Moderate-severe Peri-implantitis
Led by Nadja Naenni · Updated on 2024-05-14
120
Participants Needed
3
Research Sites
369 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
The Adjunctive Effect of Soft Tissue Augmentation Procedures of Moderate-severe Peri-implantitis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age > 18 years old (UZH, FRA) or > 21 years old (SIN), male and female
- Diagnosed with periimplantitis on at least 1 implant in function for at least 1 year
- Presence of bleeding and/or suppuration on gentle probing
- Probing depths of 6 mm
- Bone levels 3 mm apical of the most coronal portion of the intraosseous part of the implant
- Periodontal health including previously treated periodontitis patients with reduced but healthy periodontium
- Good oral hygiene with full mouth plaque score <25%
- Adequate control of inflammation with full mouth bleeding on probing <25%
- Signed informed consent form
You will not qualify if you...
- Pregnant or lactating female patient at inclusion
- Allergy or objection to porcine and bovine implantable biomaterials
- Allergy to Penicillin or NSAIDs
- Known or suspected non-compliance, drug or alcohol abuse
- Inability to follow the study procedures due to language, comprehension problems, psychological disorders, dementia, etc.
- Smoking more than 15 cigarettes a day
- Active periodontal disease
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
Department of Oral Surgery and Implantology, Centre for Dentistry and Oral Medicine (Carolinum), Johann Wolfgang Goethe-University Frankfurt
Frankfurt, Germany
Not Yet Recruiting
2
National Dental Centre Singapore
Singapore, Singapore
Not Yet Recruiting
3
Clinic of Reconstructive Dentistry, Center of Dental Medicine University of Zurich
Zurich, Switzerland
Actively Recruiting
Research Team
J
Jolanta Boruta
CONTACT
S
Silvia Rasi, Dr.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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