Influence of Implant Surface Decontamination on the Reconstructive Outcomes of Peri-implantitis
- Conditions
- Peri-Implantitis
- Registration Number
- NCT05615051
- Lead Sponsor
- Center of Implantology, Oral and Maxillofacial Surgery, Badajoz, Spain
- Brief Summary
Two groups are aimed at being investigated in three centers (CICOM, Clinica Branemark and Clinica Joan Pi)
* Test group: Group electrolytic approach (EA): Mechanical detoxification using curettes + NiTi brushes + EA (GalvoSurge) during 2 minutes
* Control group: Group hydrogen peroxide (HP): Mechanical detoxification using curettes + NiTi brushes + hydrogen peroxide 5% for 2 minutes soaked in a gauze Patients´ group selection will be randomly allocated. For patients whom their personal clinical record # ends in a number from 0 to 4 will be included in the test group, while for patients whom their personal clinical record # ends from 5-9 will be included in the control group.
The infra-osseous component will be regenerated using xenograft (Creos, NB) + autogenous bone in a ratio 1:1 harvested from the adjacent area. A resorbable membrane (Creos, NB) will be placed to compartmentalize the infra-osseous component following a poncho-like approach.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 60
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Resolution of the disease 12 months No pocket depth \>6mm, no bleeding on probing, no suppuration, no progressive bone loss
- Secondary Outcome Measures
Name Time Method Radiographic bone gain and clinical outcomes 12 months Bone gain and changes in defect angle when compared to baseline radiographic features and evolution of clinical parameters compared to baseline data
Trial Locations
- Locations (1)
Clinica CICOM
🇪🇸Badajoz, Spain
Clinica CICOM🇪🇸Badajoz, Spain