Influence of Implant Surface Decontamination on the Reconstructive Outcomes of Peri-implantitis
NCT: NCT05615051 · ACTIVE_NOT_RECRUITING
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.
Frequently Asked Questions
What is Influence of Implant Surface Decontamination on the Reconstructive Outcomes of Peri-implantitis?
Influence of Implant Surface Decontamination on the Reconstructive Outcomes of Peri-implantitis is a clinical trial registered under NCT05615051. Current status: ACTIVE_NOT_RECRUITING.
What is the status of NCT05615051?
The current status of NCT05615051 (Influence of Implant Surface Decontamination on the Reconstructive Outcomes of Peri-implantitis) is: ACTIVE_NOT_RECRUITING.
When did Influence of Implant Surface Decontamination on the Reconstructive Outcomes of Peri-implantitis start?
Influence of Implant Surface Decontamination on the Reconstructive Outcomes of Peri-implantitis started on 2022-01-01.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.